SLRHS5SVista

iHealth ® iHealth Vista Wireless Body Analysis Scale OWNER’S MANUAL TABLE OF CONTENTS INTENDED USE ........................................................................................................................................... 1 IMPORTANT NOTE FOR USERS .............................................................................................................. 1 CONTRAINDICATION ............................................................................................................................... 1 OFFLINE MEMORY .................................................................................................................................... 2 SPECIFICATIONS ........................................................................................................................................ 2 GENERAL SAFETY AND PRECAUTIONS ............................................................................................... 3 EXPLANATION OF SYMBOLS ................................................................................................................. 6 INTENDED USE The iHealth Vista Wireless Body Analysis Scale is a precision electronic instrument intended for adult use. The Scale utilizes full electronic methodology and pressure sensors to non-invasively measure body composition components automatically. The measurements are displayed and stored on an iPod touch, iPhone, or iPad with a date and time stamp. IMPORTANT NOTE FOR USERS Pregnant women need to consult their healthcare provider before use. Some physical conditions could affect hydration levels that may lead to inaccurate results. Please consult your healthcare provider for more information. Always store the iHealth Vista Wireless Body Analysis Scale in a dry place. To ensure accurate results, keep the Scale away from magnetic fields as these may adversely affect results or possibly damage the Scale. CONTRAINDICATION Never use this product in combination with medical electronic devices such as: (1) Medical electronic implants such as pacemakers. (2) Electronic life support systems such as artificial heart/lungs. (3) Portable electronic medical devices such as electrocardiographs. This product could cause these devices to malfunction posing a considerable health risk to users of these devices. OFFLINE MEMORY The Scale can store up to 200 weight results for each user. When each user’s memory is full, any new measurements will overwrite the oldest ones. SPECIFICATIONS 1. Product name: iHealth Vista Wireless Body Analysis Scale 2. Model: HS5 3. Classification: internally powered, type BF applied part (four electrodes) 4. Power: 4×1.5V AA alkaline batteries Battery life: approx. 3 months with daily usage 5. Measurement range: Body Weight: 11 lb-330 lb/5 kg-150 kg Body Fat: 5.0%-65.0% Humidity: 20 - 85%RH Scale resolution:0.2lb/0.1kg 6. Accuracy: Body Weight: ±1.1 lb/0.5 kg(5 kg-40 kg / 11-88 lb); ±1%+ 0.2 lb / 0.1 kg(40 kg-150 kg / 88-330 lb) Body Fat: ±1% 7. Operating temperature: 10°C - 35°C(50°F-95°F) 8. Operating humidity: 20 - 85%RH 9. Storage and transport temperature: -20°C - 60°C(-4°F-140°F) 10. Storage and transport humidity:10 - 95%RH GENERAL SAFETY AND PRECAUTIONS 1. Do not use the Scale on an uneven floor, a soft surface or a carpet as doing so may result in unreliable data. 2. This Wireless Body Analysis Scale is designed for adults. Infants or young children or any person who cannot stand still without assistance, should not use it. 3. Avoid using this Scale near strong magnetic fields, such as microwave ovens, etc. 4. The Scale will maintain its safety and performance features for at least 10,000 measurements or two years of use. 5. This device complies with part 15 of the FCC Rules. Its operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Cet appareil est conforme à la section 15 des réglementations de la FCC. Le fonctionnement de l’appareil est sujetaux deux conditions suivantes : (1) cet appareil ne doit pas provoquer d’interférences néfastes, et (2) cet appareil doit tolérer les interférences reçues, y compris celles qui risquent de provoquer un fonctionnement indésirable. 6. Changes or modifications not expressly approved by iHealth Lab Inc. invalidate the user’s warranty for this equipment. 7. This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: —Reorient or relocate the receiving antenna. —Increase the separation between the equipment and receiver. —Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. —Consult the dealer or an experienced radio/TV technician for help. 8. Please take attention that changes or modification not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment. 9. This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device. 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iHealth Lab Inc. Declaration We (iHealth Lab Inc.) hereby declare the device cannot use channel 12 and channel 13 for WiFi mode and end user cannot to configure it with any means Thanks,

Request for Confidentiality Date: 2015-1-25 _ Subject: Confidentiality Request for: _FCC ID: SLRHS5S Pursuant to FCC 47 CRF 0.457(d) and 0.459 and IC RSP-100, Section 10, the applicant requests that a part of the subject FCC application be held confidential. Type of Confidentiality Requested Exhibit Short Term Permanent Block Diagrams Short Term External Photos Short Term Permanent* 1 Internal Photos Short Term Permanent Operation Description/Theory of Operation Short Term Permanent Parts List & Placement/BOM Short Term Permanent Tune-Up Procedure Short Term Permanent Schematics Short Term Test Setup Photos Short Term Permanent* User’s Manual *Note: ______(Insert Explanation as Necessary)______ _ iHealth Lab Inc. has spent substantial effort in developing this product and it is one of the first of its kind in industry. Having the subject information easily available to "competition" would negate the advantage they have achieved by developing this product. Not protecting the details of the design will result in financial hardship. Permanent Confidentiality: The applicant requests the exhibits listed above as permanently confidential be permanently withheld from public review due to materials that contain trade secrets and proprietary information not customarily released to the public. Short-Term Confidentiality: The applicant requests the exhibits selected above as short term confidential be withheld from public view for a period of ___(specify number of days not to exceed 180 ) 2 ___ days from the date of the Grant of Equipment Authorization and prior to marketing. This is to avoid premature release of sensitive information prior to marketing or release of the product to the public. Applicant is also aware that they are responsible to notify ACB in the event information regarding the product or the product is made available to the public. ACB will then release the documents listed above for public disclosure pursuant to FCC Public Notice DA 04-1705. Sincerely, By: 1 - The asterisked items (*) require further justification before permanent confidentiality will be allowed. These also currently require review by the FCC under their Permit-But-Ask policy before the grant is issued and can delay completion of an application. Further justification should be added to the note above. One such example for a potted device would be: “The EUT is FULLY potted using a non-removable epoxy based material. Removal of potting material causes irreparable damage to internal circuitry. See photographs exhibits that outline the device before and after potting.” 2 - Please refer to http://acbcert.com/documents/misc-docs/Memo-Short-Term-Vs-Standard-Confidentiality.pdf for complete details.

2015-1-25

SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Page: 1 of 3 Page 1 of 3 HS5S _External Photos-FCC Application No.: SHEM1501000131CR Applicant: iHealth Lab Inc. Address of Applicant: 719 N.Shoreline Blvd, Mountain View, CA94043 Equipment Under Test (EUT): Product Name: Vista Brand Name: iHealth Model No.: HS5S FCC ID: SLRHS5S IC: 10913A-HS5S SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Page: 2 of 3 Page 2 of 3 1 Contents Page 1 CONTENTS.......................................................................................................... 2 2 EXTERNAL PHOTOS ........................................................................................ 3 SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Page: 3 of 3 Page 3 of 3 2 External Photos End

SGS-CSTC Standards Technical Services Co., Ltd . No. 1 Workshop, M-10, Middle section, Science & Technology Park, Nanshan District, Shenzhen, Guangdong, China 518057 Telephone: +86 (0) 755 2601 2053 Fax: +86 (0) 755 2671 0594 Email: [email protected] Report No.: SZEM150300093901 Rev.01 Page : 1 of 31 Authorized Signature: Jack Zhang EMC Laboratory Manager The manufacturer should ensure that all products in series production are in conformity with the product sample detailed in this report. If the product in this report is used in any configuration other than that detailed in the report, the manufacturer must ensure the new system complies with all relevant standards. Any mention of SGS International Electrical Approvals or testing done by SGS International Electrical Approvals in connection with, distribution or use of the product described in this report must be approved by SGS International Electrical Approvals in writing. The report must not be used by the client to claim product certification, approval, or endorsement by NVLAP, NIST, or any agency of the federal government. All test results in this report can be traceable to National or International Standards. “This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm . Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only.” FCC SAR TEST REPORT Application No: SZEM1503000939CR(SGS SH No.:SHEM1501000131CR) Applicant: iHealth Manufacturer/ Factory: Andon Health Co. Ltd Product Name: Vista Model No.(EUT): HS5S Trade Mark: iHealth FCC ID: SLRHS5S Standards: FCC 47CFR §2.1093 Date of Receipt: 2015-03-03 Date of Test: 2015-04-02 Date of Issue: 2015-04-16 Test Result : PASS * * In the configuration tested, the EUT detailed in this report complied with the standards specified above. SGS-CSTC Standards Technical Services Co., Ltd. Report No.: SZEM150300093901 Rev.01 Page: 2 of 31 “This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm . Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only.” REVISION HISTORY Revision Record Version Chapter Date Modifier Remark 00 2015-04-16 Original SGS-CSTC Standards Technical Services Co., Ltd. Report No.: SZEM150300093901 Rev.01 Page: 3 of 31 “This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm . Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only.” Test Summary Frequency Band Test position Test mode Max Report SAR 10g (W/kg) SAR limit (W/kg) Verdict WI-FI (2.4GHz) Front side 802.11b 0.134 4.0 PASS Approved & Released by Evan Mi SAR Manager Tested by Eason Wang SAR Engineer SGS-CSTC Standards Technical Services Co., Ltd. Report No.: SZEM150300093901 Rev.01 Page: 4 of 31 “This document is issued by the…

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Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner Scanned by CamScanner June 26, 2013 1 Acceptable Conditions for SAR Measurements Using Probes and Dipoles Calibrated under the SPEAG-TMC Dual-Logo Calibration Program to Support FCC Equipment Certification The acceptable conditions for SAR measurements using probes, dipoles and DAEs calibrated by TMC (Telecommunication Metrology Center of MITT in Beijing, China), under the Dual-Logo Calibration Certificate program and quality assurance (QA) protocols established between SPEAG (Schmid & Partner Engineering AG, Switzerland) and TMC, to support FCC (U.S. Federal Communications Commission) equipment certification are defined and described in the following. 1) The agreement established between SPEAG and TMC is only applicable to calibration services performed by TMC where its clients (companies and divisions of such companies) are headquartered in the Greater China Region, including Taiwan and Hong Kong. This agreement is subject to renewal at the end of each calendar year between SPEAG and TMC. TMC shall inform the FCC of any changes or early termination to the agreement. 2) Only a subset of the calibration services specified in the SPEAG-TMC agreement, while it remains valid, are applicable to SAR measurements performed using such equipment for supporting FCC equipment certification. These are identified in the following. a) Calibration of dosimetric (SAR) probes EX3DVx, ET3DVx and ES3DVx. i) Free-space E-field and H-field probes, including those used for HAC (hearing aid compatibility) evaluation, temperature probes, other probes or equipment not identified in this document, when calibrated by TMC, are excluded and cannot be used for measurements to support FCC equipment certification. ii) Signal specific and bundled probe calibrations based on PMR (probe modulation response) characteristics are handled according to the requirements of KDB 865664; that is, “Until standardized procedures are available to make such determination, the applicability of a signal specific probe calibration for testing specific wireless modes and technologies is determined on a case-by-case basis through KDB inquiries, including SAR system verification requirements.” b) Calibration of SAR system validation dipoles, excluding HAC dipoles. c) Calibration of data acquisition electronics DAE3Vx, DAE4Vx and DAEasyVx. d) For FCC equipment certification purposes, the frequency range of SAR probe and dipole calibrations is limited to 700 MHz - 6 GHz and provided it is supported by the equipment identified in the TMC QA protocol (a separate attachment to this document). e) The identical system and equipment setup, measurement configurations, hardware, evaluation algorithms, calibration and QA protocols, including the format of calibration certificates and reports used by SPEAG shall be applied by TMC. f) The calibrated items are only applicable to SPEAG DASY 4 and DASY 5 or higher version systems. June 26, 2013 2 3) The SPEAG-TMC agreement includes specific protocols identified in the following to ensure the quality of calibration services provided by TMC under this SPEAG- TMC Dual-Logo calibration agreement are equivalent to the calibration services provided by SPEAG. TMC shall, upon request, provide copies of documentation to the FCC to substantiate program implementation. a) The Inter-laboratory Calibration Evaluation (ILCE) stated in the TMC QA protocol shall be performed between SPEAG and TMC at least once every 12 months. The ILCE acceptance criteria defined in the TMC QA protocol shall be satisfied for the TMC, SPEAG and FCC agreements to remain valid. b) Check of Calibration Certificate (CCC) shall be performed by SPEAG for all calibrations performed by TMC. Written confirmation from SPEAG is required for TMC to issue calibration certificates under the SPEAG-TMC Dual-Logo calibration program. Quarterly reports for all calibrations performed by TMC under the program are also issued by SPEAG. c) The calibration equipment and measurement system used by TMC shall be verified before each calibration service according to the specific reference SAR probes, dipoles, and DAE calibrated by SPEAG. The results shall be reproducible and within the defined acceptance criteria specified in the TMC QA protocol before each actual calibration can commence. TMC shall maintain records of the measurement and calibration system verification results for all calibrations. d) Quality Check of Calibration (QCC) certificates shall be performed by SPEAG at least once every 12 months. SPEAG shall visit TMC facilities to verify the laboratory, equipment, applied procedures and plausibility of randomly selected certificates. 4) A copy of this document, to be updated annually, shall be provided to TMC clients that accept calibration services according to the SPEAG-TMC Dual-Logo calibration program, which should be presented to a TCB (Telecommunication Certification Body), to facilitate FCC equipment approval. 5) TMC shall address any questions raised by its clients or TCBs relating to the SPEAG- TMC Dual-Logo calibration program and inform the FCC and SPEAG of any critical issues. Change Note: Revised on June 26 to clarify the applicability of PMR and Bundled probe calibrations according to the requirements of KDB 865664. SGS-CSTC Standards Technical Services Co., Ltd. Report No.: SZEM150300093901 Appendix D Photographs 1. SAR measurement System 2. Photographs of Tissue Simulate Liquid 3. Photographs of EUT test position 4. EUT Constructional Details SGS-CSTC Standards Technical Services Co., Ltd. Report No.: SZEM150300093901 1. SAR measurement System: 2. Photographs of Tissue Simulate Liquid Photo 1: Tissue Simulant Liquid for Body 2450 NA NA SGS-CSTC Standards Technical Services Co., Ltd. Report No.: SZEM150300093901 3. Photogr…

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SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. 588 West Jindu Road,Songjiang District,Shanghai,China Telephone: +86 (0) 21 6191 5666 Fax: +86 (0) 21 6191 5678 [email protected] Report No.: SHEM150100013102 Page: 1 of 91 Parlam Zhan E&E Section Manager SGS-CSTC (Shanghai) Co., Ltd. The manufacturer should ensure that all products in series production are in conformity with the product sample detailed in this report. If the product in this report is used in any configuration other than that detailed in the report, the manufacturer must ensure the new system complies with all relevant standards. The report must not be used by the client to claim product certification, approval, or endorsement by NVLAP, NIST, or any agency of the federal government. All test results in this report can be traceable to National or International Standards. This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e-document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to the sample(s) tested and such sample(s) are retained for 90 days only 1 Cover Page RF TEST REPORT Application No.: SHEM1501000131CR Applicant: iHealth Lab Inc. FCC ID: SLRHS5S Equipment Under Test (EUT): NOTE: The following sample(s) submitted was/were identified on behalf of the client as Product Name: Vista Model No.(EUT): HS5S Standards: FCC PART 15 Subpart C: 2014 Date of Receipt: January 15, 2015 Date of Test: January 22, 2015 to January 26, 2015 Date of Issue: February 09, 2015 Test Result: Pass* *In the configuration tested, the EUT detailed in this report complied with the standards specified above. SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Report No.: SHEM150100013102 Page: 2 of 91 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e- document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to thesample(s) tested and such sample(s) are retained for 90 days only 2 Version Revision Record Version Chapter Date Modifier Remark 00 / February 09, 2015 / Original Authorized for issue by: Engineer Eddy Zong Print Name Clerk Susie Liu Print Name Reviewer Keny Xu Print Name SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Report No.: SHEM150100013102 Page: 3 of 91 This document is issued by the Company subject to its General Conditions of Service printed overleaf, available on request or accessible at www.sgs.com/terms_and_conditions.htm and, for electronic format documents, subject to Terms and Conditions for Electronic Documents at www.sgs.com/terms_e- document.htm. Attention is drawn to the limitation of liability, indemnification and jurisdiction issues defined therein. Any holder of this document is advised that information contained hereon reflects the Company’s findings at the time of its intervention only and within the limits of Client’s instructions, if any. The Company’s sole responsibility is to its Client and this document does not exonerate parties to a transaction from exercising all their rights and obligations under the transaction documents. This document cannot be reproduced except in full, without prior written approval of the Company. Any unauthorized alteration, forgery or falsification of the content or appearance of this document is unlawful and offenders may be prosecuted to the fullest extent of the law. Unless otherwise stated the results shown in this test report refer only to thesample(s) tested and such sample(s) are retained for 90 days only 3 Test Summary Test Item FCC Requirement Test method Result Antenna Requirement FCC Part 15, Subpart C Section 15.203/15.247 (c) --- PASS AC Power Line Conducted Emission FCC Part 15, Subpart C Section 15.207 ANSI C63.10 (2009) Section 6.2 N/A Minimum 6dB Bandwidth FCC Part 15, Subpart C Section 15.247 (a)(2) ANSI C63.10 (2009) Section 6.9.1 PASS Conducted Peak Output Power FCC Part 15, Subpart C Section 15.247 (b)(3) ANSI C63.10 (2009) Section 6.10.2 PASS Power Spectrum Density FCC P…

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SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Page: 1 of 4 Page 1 of 4 HS5S _Test Setup Photos-FCC Application No.: SHEM1501000131CR Applicant: iHealth Lab Inc. Address of Applicant: 719 N.Shoreline Blvd, Mountain View, CA94043 Equipment Under Test (EUT): Product Name: Vista Brand Name: iHealth Model No.: HS5S FCC ID: SLRHS5S IC: 10913A-HS5S SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Page: 2 of 4 Page 2 of 4 1 Contents Page 1 CONTENTS............................................................................................................... 2 2 EQUIPMENT UNDER TEST PICTURES ............................................................ 3 2.1 Radiated Emission Test Setup ............................................................. 3 SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Page: 3 of 4 Page 3 of 4 2 EQUIPMENT UNDER TEST PICTURES 2.1 Radiated Emission Test Setup Below 30MHz: 30MHz to 1GHz SGS-CSTC Standards Technical Services (Shanghai) Co., Ltd. Page: 4 of 4 Page 4 of 4 Above 1GHz End