TVF-L3P-T-RFS-V10Thigh RF Stimulation Unit

NESS L300 Plus System User’s Guide Rx Only II NESS L300 Plus User’s Guide Copyright © 2010, Bioness Inc All Rights Reserved No part of this publication may be reproduced, transmitted, transcribed, stored in a retrieval system, or translated into any language or any computer language, in any form or by any third party, without the prior written permission of Bioness Inc. Trademarks NESS ® , NESS L300™, NESS L300 Plus™ Intelli-Gait™, Intelli-Sense Gait Sensor™, Bioness ® , the Bioness Logo and LiveOn™ are trademarks of Bioness Inc. | www.bioness.com | Rx Only Use of the symbols ® and ™ herein refers to the registration status of trademarks in the U.S. only. These trademarks may also be registered in other countries. Patents Pending Aspects of this device are covered by several patents and patent applications. Disclaimer Bioness Inc and its affiliates shall not be liable for any injury or damage suffered by any person, either directly or indirectly, as a result of the unauthorized use or repair of Bioness Inc products. Bioness Inc does not accept any responsibility for any damage caused to its products, either directly or indirectly, as a result of use and/or repair by unauthorized personnel. Environmental Policy Service personnel are advised that when changing any part of the NESS L300 Plus, care should be taken to dispose of those parts in the correct manner; where applicable, parts should be recycled. For more detailed information regarding these recommended procedures, please contact Bioness Inc. Bioness Inc is committed to continuously seeking and implementing the best possible manufacturing procedures and servicing routines. Worldwide Corporate Office Bioness Inc 25103 Rye Canyon Loop Valencia, CA 91355 USA Telephone: 800-211-9136 Email: [email protected] Website: www.bioness.com Manufactured by Bioness Neuromodulation Ltd. A Bioness Inc Company 19 Ha’Haroshet Street PO Box 2500 Industrial Zone Ra’Anana 43654, Israel Bioness Customer Support: Telephone: (800) 211-9136, Option 2; or (661) 362-4850, Option 2. III Contents Chapter 1: Introduction ........................................................................ 1 Chapter 2: For Your Health and Safety ............................................... 3 Indications for Use ............................................................................................ 3 Contraindications .............................................................................................. 3 Warnings .......................................................................................................... 4 Precautions ....................................................................................................... 4 Adverse Reactions ........................................................................................... 7 Skin Care Guidelines ........................................................................................ 8 Chapter 3: Environmental Conditions that Affect Use ...................... 11 Radio Frequency (RF) Communication ............................................................ 11 Conformity Certification .............................................................................. 12 Travel ................................................................................................................ 12 Chapter 4: Your NESS L300 Plus System Kit ..................................... 13 Contents ........................................................................................................... 13 System Components .................................................................................. 13 L300 Accessories ....................................................................................... 14 L300 Plus Accessories ............................................................................... 16 L300 Plus Upgrade Kit ...................................................................................... 17 Contents ..................................................................................................... 17 Chapter 5: System Components and Accessories............................ 19 L300 Functional Stimulation (FS) Cuff ............................................................. 19 Locator ........................................................................................................ 20 RF Stim Unit Cradle .................................................................................... 20 Strap ........................................................................................................... 20 Electrode Bases and Surface Electrodes .................................................. 20 L300 RF Stim Unit ............................................................................................ 21 IV NESS L300 Plus Thigh FS Cuff .................................................................................................. 23 Distal and Proximal Panels ......................................................................... 24 Elongation Bar ............................................................................................ 24 Straps ......................................................................................................... 24 Surface Electrodes ..................................................................................... 24 Thigh RF Stim Unit ........................................................................................... 25 Gait Sensor ....................................................................................................... 27 L300 Plus Control Unit ...................................................................................... 29 Control Unit Operating Buttons ................................................................... 30 Control Unit Operating Modes .................................................................... 30 Control Unit Digital Display and Indicator Lights .............…

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35 Chapter 5 - System Components and Accessories L300 Accessories L300 Hydrogel Electrodes The L300 hydrogel electrodes are used with the L300 FS Cuff. See Figure 9. Two hydrogel electrodes are used to deliver stimulation from the L300 RF Stim Unit to the muscles in the lower leg. Each hydrogel electrode attaches to a hydrogel electrode base. The side of the electrode with the grid faces the electrode base. Do not use the L300 FS Cuff without electrodes. Always replace the plastic covers on the hydrogel electrodes between uses. Hydrogel Electrode Figure 9: Hydrogel electrode, front (left) and back (right). Caution: Change the electrodes every two weeks. Caution: Only use electrodes provided by Bioness Inc. 36 NESS L300 Plus User’s Guide L300 Hydrogel Electrode Bases The hydrogel electrode bases are for use with the L300 FS Cuff. See Figure 10. Your clinician will determine the best placement for the hydrogel electrode bases. The hydrogel electrodes attach to the hydrogel electrode bases. Always attach the grid side of the hydrogel electrodes to the hydrogel electrode bases. Do not move the electrode bases once your clinician has fit them, other than to replace them. The hydrogel electrode bases need to be replaced approximately once every two years.. Hydrogel Electrode Base Figure 10: Hydrogel electrode base. 37 Chapter 5 - System Components and Accessories L300 Cloth Electrodes The L300 cloth electrodes are used to deliver stimulation from the L300 RF Stim Unit to the lower leg muscles. See Figure 11. They are designed to be skin friendly and provide an alternative for people who do not prefer the L300 hydrogel electrodes. They are also for people who have sensitivities to the L300 hydrogel electrodes or other known sensitivities (for example, allergy or skin sensitivity to tape/adhesive). The L300 FS Cuff uses two cloth electrodes. Each one snaps to a cloth electrode base. The L300 cloth electrodes must be wet before use and after every three to four hours of use. If the L300 FS Cuff is removed for more than one hour, the cloth electrodes need to be rewet. Allow the cloth electrodes to dry between uses. Do not use the L300 FS Cuff without electrodes. Cloth Electrode Figure 11: L300 cloth electrode, front (left) and back (right). Caution: Change the electrodes every two weeks. Caution: Only use electrodes provided by Bioness Inc. 38 NESS L300 Plus User’s Guide L300 Cloth Electrode Bases The L300 cloth electrode bases are for use with the L300 FS Cuff. See Figure 12. Your clinician will determine the best placement for the cloth electrode bases. The L300 cloth electrodes snap to the L300 cloth electrode bases. Do not move the electrode bases once your clinician has fit them, other than to replace them. Cloth electrode bases need to be replaced approximately once every two years. Cloth Electrode Base Figure 12: L300 cloth electrode base. 39 Chapter 5 - System Components and Accessories Wrist Strap, Neck Strap, and Belt Pouch The wrist strap, neck strap, and belt pouch are used to carry the L300 Plus Control Unit. The wrist and neck straps loop through the top of the Control Unit. See Figure 13. Wrist StrapBelt Pouch Neck Strap Figure 13: L300 Plus Control Unit carrying options. 40 NESS L300 Plus User’s Guide Replacement Battery, Gait Sensor The L300 Plus System Kit includes a replacement coin battery for the Gait Sensor. The battery will need to be replaced approximately every six months. See Figure 14. Gait Sensor Battery Figure 14: Gait Sensor battery. 41 Chapter 5 - System Components and Accessories Figure 15: Placement of the Gait Sensor pad and pressure sensor. Gait Sensor Pads The Gait Sensor pads are used to stabilize the Gait Sensor pressure sensor in the shoe. See Figure 15. One Gait Sensor pad is placed under the insole of the shoe of the affected leg. The Gait Sensor pressure sensor is then placed on top of the Gait Sensor pad. Finally, the insole of the shoe is lowered to cover both the pressure sensor and the Gait Sensor pad. Place the adhesive side of the Gait Sensor pad down. Pressure Sensor Gait Sensor Pad 42 NESS L300 Plus User’s Guide Shoe Spacers The shoe spacers are used to protect the rim of the shoe from the clamp of the gait sensor transmitter. See Figure 16. One shoe spacer is placed over the inner clamp of the Gait Sensor. Figure 16: Attaching the shoe spacer. Phillips Screwdriver The Phillips screwdriver is used to replace the Control Unit and Gait Sensor batteries. Shoe Spacer Inner Clamp 43 Chapter 5 - System Components and Accessories Figure 17: L300 Plus System charger set L300 Plus Accessories L300 Plus System Charger Set The L300 Plus system charger set is used to simultaneously charge the L300 RF Stim Unit, the Thigh RF Stim Unit, and the L300 Plus Control Unit. The system charger set includes a "W" cable and a charger, and a set of interchangeable blades for international outlets. The "W" cable and the charger must be assembled for use. See Figure 17. 44 NESS L300 Plus User’s Guide Thigh FS Cuff Distal Panel Subassembly, Large The Thigh FS Cuff has two panels: a proximal panel and a distal panel. The distal panel includes the cradle for the Thigh RF Stim Unit. The distal panel is available in two sizes: small and large. The Thigh FS Cuff in your L300 Plus System Kit features the small distal panel. A large distal panel subassembly is also provided, if needed. See Figure 18. Your clinician will measure your thigh circumference during your L300 Plus fitting session and determine the appropriate sized distal panel for your Thigh FS Cuff. If the large distal panel subassembly is needed, your clinician will reconfigure your Thigh FS Cuff. Figure 18: Thigh FS Cuff distal panel subassembly, large. 45 Chapter 5 - System Components and Accessories Thigh FS Cuff Elongation Bar Lock Set During your L300 Plus fitting session, your clinician will adjust the elongation bar on the Thigh FS Cuff. The elongation bar is used to adjust the distance between the Thigh FS Cuff…

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81 Chapter 8 - Operating the L300 Plus Control Unit Component Maintenance and Cleaning Charging the Batteries When a system component has a low battery, the Control Unit will beep and the component indicator light will flash YELLOW. See Figure 43. When an RF Stim Unit battery charge level is low, the RF Stim Unit status light will also flash YELLOW. See inset in Figure 43. When the Gait Sensor battery is low, the Control Unit low-battery audio alert will become more persistent as the battery weakens. 9 Low Battery, Thigh RF Stim Unit Low Battery, L300 RF Stim Unit Low Battery, Gait Sensor Low Battery, Control Unit Low Battery, RF Stim Unit Figure 43: Low battery FLASHING YELLOW indicators. 82 NESS L300 Plus User’s Guide To charge the batteries in the Control Unit and RF Stim Units: 1. Open the cover of the charging ports (found at the bottom of the Control Unit and at the top of the RF Stim Units). See Figure 44. Figure 44: Charging ports: Control Unit and RF Stim Units. L300 RF Stim Unit Charging Port Cover Cover Control Unit Charging Port Cover Thigh RF Stim Unit Charging Port 83 Chapter 9 - Component Maintenance and Cleaning 2. Connect the system charger set to the Control Unit and both RF Stim Units. See Figure 45. Figure 45: Charging setup. System Charger Set Note: 0.6-cm (1/4-in.) gap is normal 84 NESS L300 Plus User’s Guide 3. Plug the system charger set into a wall socket. 4. Verify that the rotating GREEN circle appears in the Control Unit digital display, and the status light on the both RF Stim Units is alternately flashing YELLOW and GREEN. 5. The charging process will continue until a horizontal GREEN line appears in the Control Unit digital display and the status light on both RF Stim Units is solid GREEN. See figures 46 and 47. The charging process should last approximately three hours. The Control Unit and RF Stim Units can remain connected to the charger after charging is complete. Note: It is possible to charge the Control Unit and RF Stim Units separately, but Bioness recommends that they be charged at the same time. Caution: The batteries must be charged before first use, daily, and after extended storage. Caution: Only the Control Unit and RF Stim Unit batteries are rechargeable. Caution: Remove the L300 FS Cuff and Thigh FS Cuff before charging the batteries. Caution: Do not use the RF Stim Units or the Control Unit while charging. 85 Chapter 8 - Operating the L300 Plus Control Unit Figure 46: Control Unit charging displays. Horizontal GREEN Line: Control Unit Fully Charged Rotating GREEN Circle: Control Unit Charging Note: If the Control Unit battery is completely discharged, a “b” (for boot) will flash for a few seconds in the Control Unit digital display when charging is started. Figure 47: RF Stim Unit charging displays. Status Light Alternately Flashing GREEN and YELLOW: RF Stim Unit Charging Status Light Solid GREEN: RF Stim Unit Fully Charged 86 NESS L300 Plus User’s Guide Replacing the Batteries Replacing the RF Stim Unit Batteries Each RF Stim Unit has a rechargeable battery. The battery should be replaced approximately every two years by a Bioness certified technician. Replacing the Gait Sensor Battery The battery in the Gait Sensor is not rechargeable. It should be replaced approximately every six months. The Gait Sensor indicator on the Control Unit will begin to flash YELLOW approximately two weeks before the Gait Sensor completely loses its charge. The Control Unit will also emit an alarm. To replace the Gait Sensor battery (Lithium coin cell, CR2430): 1. Unscrew the two screws from the battery cover. See Figure 48. Slide the cover out. Figure 48: Replacing the Gait Sensor battery. Screws Note: If you are unable to replace the battery yourself, your local watchmaker or battery supply store should be able to assist. Battery Cover 87 Chapter 9 - Component Maintenance and Cleaning 2. Note the “+” orientation of the old battery. 3. Remove the old battery and properly dispose of it according to your local environmental regulations. 4. Insert the new battery. The “+” should face outward. 5. Slide the cover back into place, and tighten the screws. 6. Press the Gait Sensor pressure sensor to activate the sensor. Remove the old battery, and properly dispose of it according to your local environmental regulations. Replacing the L300 Plus Control Unit Battery The battery in the Control Unit is a rechargeable AAA battery. It should be replaced approximately every two years. To replace the Control Unit battery (AAA NiMH 1.2 V): 1. Remove the screw from the battery cover on the back of the Control Unit. See Figure 49. (The screw may be under a small label. If so, gently peel off one end of the label. Reapply the label after the battery is replaced.) 2. Remove the battery cover. 3. Note the "+/-" orientation of the old battery. 88 NESS L300 Plus User’s Guide Figure 49: Replacing the Control Unit battery. Remove the old battery, and properly dispose of it according to your local environmental regulations. 4. Insert the new rechargeable battery in the proper "+/-" orientation. 5. Slide the cover into place, and tighten the screw. 6. Fully charge the new battery before first use. Caution: Use of a non-rechargeable AAA battery can damage the Control Unit. Note: If you are unable to replace the battery, your local watchmaker or battery supply store should be able to assist. Control Unit Battery Battery Cover Screw 89 Chapter 8 - Operating the L300 Plus Control Unit Replacing the L300 Hydrogel Electrodes You will need to replace the hydrogel electrodes at least every two weeks. Caution: Use only NESS L300 electrodes supplied by Bioness. Caution: Do not use your NESS L300 without electrodes. To replace the hydrogel electrodes: 1. Turn off the L300 Plus Control Unit. 2. Gently pull the used L300 hydrogel electrodes from the hydrogel electrode bases. Be careful not to detach the electrode bases from the L300 FS Cuff. See Figure 50. 3. If necessary, clean the electrode bases w…

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Declaration of Authorization We Name: Bioness Neuromodulation Ltd.-- A Bioness Inc Company Address: 19 Ha’haroshet street, P.O.Box 2500 City: Ra’anana 43654 Country: Israel Declare that: Name Representative of agent: ............. (1) Agent Company name: Hermon Laboratories Ltd. Address: Harakevet Industrial Zone City: Binyamina 30500 Country Israel Is authorized to apply for Certification of the following product(s): Product description: ... RF Stimulation Unit Type designation: ... Thigh RF Stimulation Unit Trademark: ... NESS L300 Plus on our behalf. Date: 06/24/2010 Name: Eyal Lasko ...... . (2) Function: Project manager Signature: ................ Notes: (1): Required for FCC application (2): For FCC it must be the Grantee Code “owner” or the authorized agent.

FCC, Request for non-disclosure Date: 16-Jul-10 RF_501, Issue 6 Page 1 of 1 Company Name: Bioness Neuromodulation Ltd.- A Bioness Inc Company Address : 19 Ha’haroshet street, P.O.Box 2500 City: Ra’anana 43654 Country: Israel To: Telefication B.V ., Dept. FCC TCB Edisonstraat 12A 6902 PK ZEVENAAR The Netherlands Subject: Request for confidentiality FCC ID: TVF-L3P-T-RFS-V10 Reference number: ###### Dear FCC TCB, 1. Long-Term Confidentiality Pursuant to 47 CFR Section 0.459(a) & (b), we hereby requests non-disclosure and confidential treatment of the following materials submitted in support of FCC certification application: Bill(s) of Material Block Diagrams Operational Description Schematic Diagrams Tune-up Procedure Above materials contain secrets, proprietary and technical information, which would customarily be guarded from competitors under 47 CFR, section 0.457(d)(2). Disclosure or publication or any portion of this company confidential material to other parties could cause substantial competitive harm and provide unjustified benefits for competitors. 2. Short-Term Confidentiality (STC) Pursuant to Public Notice DA 04-1705 of the Commission’s policy, in order to comply with the marketing regulations in 47 CFR §2.803 and the importation rules in 47 CFR §2.1204, a pplicant hereby requests Short-Term Confidential treatment of the following materials (note 1): Internal Photos User’s Manual Test Set-up Photos External Photos Justification: Planned Release Date STC: (notes 2, 3, 4, 5) Date: July 1, 2010 Name and signature of applicant: Eyal Lasko Notes: 1) A document or type of document can only have ONE type of confidentiality! 2) Short-Term confidentiality is in principle for 45 days from date of grant; it can be extended max 3 times (total time 180 days max.)! 3) FCC must be informed when marketing begins earlier. 4) Release takes place automatically thus extension must be requested in time. Telefication does not remind you of this! 5) Request for extension or for release must be received by Telefication at least 7 days before date of actual marketing or before expiration of the STC period

Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 1 of 4 EXTERNAL PHOTOGRAPHS This document contains 3 photographs Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 2 of 4 Photograph No.1 RF stimulation unit general view Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 3 of 4 Photograph No.2 RF stimulation unit front view Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 4 of 4 Photograph No.3 RF stimulation unit rear side view

Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 1 of 2 LABEL LOCATION The label shown below is affixed on the rear panel of the Thigh RF Stimulation Unit. Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 2 of 2 Label location on the unit rear panel The label shown in the page 1 with FCC ID:TVF-L3P-T-RFS-V10, will be located here. The part 15 statement required by FCC rules, paragraph 15.19 (a)(3), is inserted into the User_guide_20763, paragraph “Conformity Certification”, page 12, provided to the user together with each unit.

Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 1 of 5 INTERNAL PHOTOGRAPHS This document contains 4 photographs Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 2 of 5 Photograph No.1 RF stimulation unit internal view Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 3 of 5 Photograph No.2 RF stimulation unit PCB front view Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 4 of 5 Photograph No.3 RF stimulation unit PCB rear side view Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 5 of 5 Photograph No.4 RF stimulation unit antenna close view

Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 1 of 1 RF exposure information according to FCC CFR 47 part 15, §15.247(i), part 2, §2.1093 The stimulation unit is a portable device operating in 2401-2482 MHz band. No SAR evaluation required if a transmitter power is below the following low threshold: 60/f (GHz) [mW] = 60/2.44 [mW] = 24.6 [mW]. Tunable range, GHz Flow Fhigh Center of tunable band, GHz 60/f SAR limitation, mW 2.401 2.482 2.441 24.6 Maximum measured transmitter power: Pout conducted, mW Maximum antenna gain, dBi Pout EIRP, mW 3.2 1.5 4.5 Threshold for no SAR evaluation is 24.6 mW, maximum measured Tx power is 3.2 mW – conducted and 4.5 mW- EIRP. Conclusion: No SAR evaluation is required since the maximum transmitter output power, both conducted and radiated, is below the FCC threshold.

Hermon Laboratories Ltd. Harakevet Industrial Zone, Binyamina 30500, Israel Tel. +972-4-6288001 Fax. +972-4-6288277 E-mail: [email protected] Page 1 of 81 Report ID: BIORAD_FCC.20763_rev1.doc Date of Issue: 5/23/2010 Electrical 839.01 TEST REPORT ACCORDING TO: FCC CFR 47 PART 15 Subpart C, §15.247 and RSS-210, Issue 7, Annex 8 FOR: Bioness Neuromodulation Ltd. - A Bioness Inc Company Trade mark: NESS L300 Plus Model: Thigh RF Stimulation Unit This report is in conformity with ISO/ IEC 17025. The "A2LA Accredited" symbol endorsement applies only to the tests and calibrations that are listed in the scope of Hermon Laboratories accreditation. The test results relate only to the items tested. This test report shall not be reproduced in any form except in full with the written approval of Hermon Laboratories Ltd. Report ID: BIORAD_FCC.20763_rev1.doc Date of Issue: 5/23/2010 Page 2 of 81 Table of contents 1 Applicant information..................................................................................................................................................... 3 2 Equipment under test attributes .................................................................................................................................... 3 3 Manufacturer information .............................................................................................................................................. 3 4 Test details.................................................................................................................................................................... 3 5 Tests summary.............................................................................................................................................................. 4 6 EUT description............................................................................................................................................................. 5 6.1 General information....................................................................................................................................................... 5 6.2 Ports and lines .............................................................................................................................................................. 5 6.3 Support and test equipment .......................................................................................................................................... 5 6.4 Operating frequencies ................................................................................................................................................... 5 6.5 Changes made in the EUT ............................................................................................................................................ 5 6.6 Test configuration.......................................................................................................................................................... 6 6.7 Transmitter characteristics ............................................................................................................................................ 7 7 Transmitter tests according to 47CFR part 15 subpart C and RSS-210 Annex 8 requirements................................... 8 7.1 Minimum 6 dB bandwidth .............................................................................................................................................. 8 7.2 Peak output power ...................................................................................................................................................... 13 7.3 Field strength of spurious emissions ........................................................................................................................... 20 7.4 Peak spectral power density ....................................................................................................................................... 51 7.5 Conducted emissions .................................................................................................................................................. 57 7.6 Radiated emission measurements .............................................................................................................................. 60 8 APPENDIX A Test equipment and ancillaries used for tests....................................................................................... 66 9 APPENDIX B Measurement uncertainties................................................................................................................... 68 10 APPENDIX C Test laboratory description ................................................................................................................... 69 11 APPENDIX D Specification references ....................................................................................................................... 69 12 APPENDIX E Test equipment correction factors......................................................................................................... 70 13 APPENDIX F Abbreviations and acronyms................................................................................................................. 81 Report ID: BIORAD_FCC.20763_rev1.doc Date of Issue: 5/23/2010 Page 3 of 81 1 Applicant information Client name: Bioness Neuromodulation Ltd. - A Bioness Inc Company Address: P.O.Box 2500, 19 Ha’haroshet street, Ra’anana 43654, Israel Telephone: +972 9790 7100 Fax: +972 9748 5740 E-mail: [email protected] Contact name: Mr. Eyal Lasko 2 Equipment under test attributes Product: RF Stimulation Unit Trade mark: NESS L300 Plus Model(s): Thigh RF Stimulation Unit Serial number: Thigh RFS 100 Hardware version: 1.3 Software release: 1.0.3 Receipt date 5/4/2010 3 Manufacturer information Manufacturer name: Bioness Neuromodulation Ltd. - A Bioness Inc Company Address: P.O.Box 2500, 19 Ha’haroshet street,…

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Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 1 of 6 SETUP PHOTOGRAPHS This document contains 5 photographs Bioness Neuromodulation Ltd. - A Bioness Inc Company FCC ID:TVF-L3P-T-RFS-V10 Page 2 of 6 Photograph No.1 Setup for spurious emission field strength measurements below 30 MHz in the anechoic chamber Bioness Neuromodulation L…

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