
Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.
Health-nurturing device COLLATERAL KING LW-360 Technical Data Sheet Input Voltage AC110∽240V/50Hz incoming current AC1.5A output power DC19V/3A working voltage DC12V∽24V working current DC3A operating power 11∽19V*A Handle output voltage DC1.2∽1.5V Handle input current DC<10mA Handle output current DC<10mA operating temperature 5∽40°C Preparation before use Safety precautions The following situations are prohibited: Suffering from bleeding tendency diseases, acute suppurative diseases, acute arthritic infections, skin diseases, purpura, infectious diseases Disease is disabled. Malignant tumors, breast fibromas, uterine fibroids, ovarian cysts and polyps are prohibited Severe hypertension, heart disease, pulmonary hypertension, pulmonary embolism, venous embolism are contraindicated. Metal implantation in vivo (e.g., artificial joint, plate and screw for fracture treatment, etc.) and human body counterfeiting are prohibited. Have a history of heart surgery (pacemaker, heart stent, heart bypass, etc.) or do another major within one year Surgery is prohibited. Pregnant women and infants are forbidden. 1Matters needing attention after conditioning: Pay attention to warm, conditioning after 3 to 5 hours do not blow air conditioning, fans, do not bathe, shampoo, contact with cold water. Adjust the diet. During the conditioning period, eat more light food and drink more water, and do not eat cold, spicy and stimulating food. Do not drink large amounts of alcohol. Pay attention to rest. Fatigue, fever, dry mouth and other improving reactions may occur after conditioning, so it is not suitable to work a lot or exercise vigorously. Move, get plenty of rest, restore body function. Instrument installation power connection Take out the power adapter, connect the adapter power cord according to the figure above, and first insert the DC head into the DC on the right of the instrument Power socket, plug into the mains socket; If the power adapter indicator is on, the power supply is normal. Install a professional handle The conditioning process of the magnetic water oxygen therapy instrument requires the simultaneous use of two special handles, which are made of high purity brass oxygen. Chemical process, in the heat conduction and magnetic conductivity performance is better than other metals, the following is the operation process: Prepare 2 pieces of cotton cloth Prepare a special handle Prepare special silicone sleeve Smooth the cotton cloth and place the handle in the middle of the gauze The cotton around the handle is raised to wrap the handle Install the silicone sleeve from bottom to top to tighten the handle Assemble the handle of the silicone sleeve Connect special handle 1. Unscrew the two assembled handles separately from the water addition nut, and carefully add 50∽60 ° C hot water, tighten the nut to prevent the water inside the handle from leaking out. 2. After the two handles are ready, connect the instrument and the two handles with each other using a special connection wire The use of methods Start the instrument 1、After the power supply and handle are connected, press the power switch, and the instrument indicator light indicates red light operation interface 2、After starting the instrument, the screen appears the startup LOGO page jumps to the animation interface. When the interface jumps to "the device has started", the next step, please connect the WIFI Connect to WIFI 3、Click and long press on the top of the upper right corner of the display screen, slide out of the WiFi connection interface, click and long press the icon of WiFi, the interface of the name of WiFi connection pops up, click the name of the required WiFi connection, enter the password, the WiFi connection is displayed, click to return to the WiFi connection interface, and enter the startup interface Conditioning options 1. Enter the instrument conditioning operation interface, the control unit can be divided into conditioning options, strength control, start and stop control. 2. Conditioning Options According to the conditioning of different functional parts of the human body, the instrument provides 9 options. 3. Strength control contains three options: frequency, waveform, and intensity, which can be adjusted to feel comfortable on the basis of the default value Proper gear position. 4. Start and stop control the current data indicates the output state of the device. After the host starts the output, the strength increases when the host runs normally Large, the smaller the data value Two-dimensional code is used to scan for login. The instrument needs to scan for login before it can be operated. A switch button is used to control the start/stop of the instrument. The color is green when the instrument is started. When paused, the color is red. Maintenance and custody Maintenance Precautions 1. Use a special power adapter to avoid damage caused by power supply problems 2. When clicking the touch screen, avoid touching with water on the hand to prevent liquid from flowing into the touch screen 3. In the process of It is forbidden to directly touch the two handles together. When the handle is touched together, the instrument will detect it within a certain period of time, and the "Current data" will display the "ERROR" warning mark and emit the bee-ringing alarm sound. Work environment 1. The instrument should be placed in a dry and clean position, avoiding direct sunlight and severe vibration, with a temperature requirement of 5∽40 ° C, humidity ≦ 80%, and no electromagnetic interference 2. Liquid shall not flow into the equipment during the work, so as not to cause damage to the internal circuit NOTE: 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 use…
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Shenzhen Xudonghui Health Management Co., Ltd. 303 HoudePinyuan, No. 48 Xuefu Road, Yuegui Community, Yuehai Street, Nanshan District, Shenzhen, China Agent Authorization Company: Shenzhen Xudonghui Health Management Co., Ltd. Address: 303 HoudePinyuan, No. 48 Xuefu Road, Yuegui Community, Yuehai Street, Nanshan District, Shenzhen, China Product Name: Health-nurturing device Model Number(s): LW-360 Product Description: Health-nurturing device We authorize MiCOM Labs Inc., 575 Boulder Court, Pleasanton, California 94566, USA, to act on our behalf on all matters concerning the certification of above named equipment. We declare that MiCOM Labs Inc. is allowed to forward all information related to the approval and certification of equipment to the regulatory agencies as required and to discuss any issues concerning the approval application. Any and all acts carried out by MiCOM Labs on our behalf shall have the same effect as acts of our own. Signature: Date: Aug. 05, 2022 Name: Cao Yanhui Title: General Manager Company: Shenzhen Xudonghui Health Management Co., Ltd.
ShenzhenXudonghuiHealthManagementCo.,Ltd. 303HoudePinyuan,No.48XuefuRoad,YueguiCommunity,YuehaiStreet,Nanshan District,Shenzhen,China OfficeofEngineeringTechnology FederalCommunicationsCommission 7435OaklandMillsRoad Columbia,MD21046 USA Date:Aug.05,2022 Subject;RequestforConfidentiality FCCID:2A76ELW-360 ToWhomItMayConcern, PursuanttotheprovisionsoftheCommission’srulesTitle47Sections§0.457and§0.459,we arerequestingtheCommissiontowithholdthefollowingattachment(s)asconfidential documentsfrompublicdisclosureindefinitely. Thesedocumentscontaindetailedsystemandequipmentdescriptionsandareconsideredas proprietaryinformationinoperationoftheequipment.Thepublicdisclosureofthesedocuments mightbeharmfultoourcompanyandwouldgivecompetitorsanunfairadvantageinthemarket. SchematicDiagram BlockDiagram OperationalDescription PartsList Itisourunderstandingthatallmeasurementtestreports,FCCIDlabelformatand correspondenceduringthecertificationreviewprocesscannotbegrantedasconfidential documentsandthisinformationwillbeavailableforpublicreviewoncethegrantofequipment authorizationisissued. Sincerely, Signature: Name:CaoYanhui Title:GeneralManager
Report No.: AGC14609220701AP02 Page 1 of 4 EXTERNAL PHOTOS All VIEW OF EUT TOP VIEW OF EUT Report No.: AGC14609220701AP02 Page 2 of 4 BOTTOM VIEW OF EUT FRONT VIEW OF EUT Report No.: AGC14609220701AP02 Page 3 of 4 BACK VIEW OF EUT LEFT VIEW OF EUT Report No.: AGC14609220701AP02 Page 4 of 4 RIGHT VIEW OF EUT ****************************************End of Report****************************************
FCC ID Label Location 30mm*20mm FCC ID: 2A76ELW-360 This device complies with Part 15 of the FCC Rules. 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.
Report No.: AGC14609220701AP02 Page 1 of 6 INTERNAL PHOTOS OPEN VIEW OF EUT VIEW OF ADAPTER Report No.: AGC14609220701AP02 Page 2 of 6 ANTENNA CLOSE-UP PHOTO-1 INTERNAL VIEW OF EUT (FIGURE 1) Antenna Report No.: AGC14609220701AP02 Page 3 of 6 INTERNAL VIEW OF EUT (FIGURE 2) INTERNAL VIEW OF EUT (FIGURE 3) Report No.: AGC14609220701AP02 Page 4 of 6 INTERNAL VIEW OF EUT (FIGURE 4) INTERNAL VIEW OF EUT (FIGURE 5) Report No.: AGC14609220701AP02 Page 5 of 6 INTERNAL VIEW OF EUT (FIGURE 6) INTERNAL VIEW OF EUT (FIGURE 7) Report No.: AGC14609220701AP02 Page 6 of 6 INTERNAL VIEW OF EUT (FIGURE 8) ****************************************End of Report****************************************
RF EXPOSURE EVALUATION 1. PRODUCT INFORMATION Product Description Health-nurturing device Test Model LW-360 FCC ID 2A76ELW-360 2. EVALUATION METHOD AND LIMIT Human exposure to RF emissions from mobile devices (47 CFR §2.1091) may be evaluated based on the MPE limits adopted by the FCC for electric and magnetic field strength and/or power density, as appropriate, since exposures are assumed to occur at distances of 20 cm or more from persons. LIMITS FOR GENERAL POPULATION / UNCONTROLLED EXPOSURE Frequency Range (MHz) E-field Strength (E) (V/m) Magnetic Field Strength (H) (A/m) Power Density (S) (mW/cm 2 ) Averaging Time |E| 2 , |H| 2 or S (Minutes) 0.3 -- 1.34 614 1.63 (100)* 30 1.34 -- 30 824/f 2.19/f (180/f 2 )* 30 30 -- 300 27.5 0.073 0.2 30 300 -- 1500 -- -- f/1500 30 1500 -- 100,000 -- -- 1.0 30 *Note: 1. f= Frequency in MHz * Plane-wave Equivalent Power Density 2. The averaging time for General Population/Uncontrolled exposure to fixed transmitters is not applicable for mobile and portable transmitters. See 47 CFR §§2.1091 and 2.1093 on source-based time-averaging requirement for mobile and portable transmitters. S=PG/4πR² Where: S=power density P=power input to antenna G=power gain of the antenna in the direction of interest relative to an isotropic radiator R=distance to the center of radiation of the antenna CALCULATION A minimum test separation distance ≥ 20 cm is required between the antenna and radiating structures of the device and nearby persons to apply mobile device exposure limits. The distance must be at least 20 cm and fully supported by the operating and installation configurations of the transmitter and its antenna(s), according to the source-based time-averaged maximum power requirements of § 2.1091(d)(2). In cases where cable losses or other attenuations are applied to determine compliance, the most conservative operating configurations and exposure conditions must be evaluated. Antenna Gain=1dBi (Numeric 2.24), π=3.14 Note: 1. Only the worst case recorded. Frequency Output Power Output Power Power Density Power Density Limit MHz dBm mW mW/cm 2 mW/cm 2 2412 15.35 34.28 0.0068 1
Page 1 of 79 Report No.: AGC14609220701FE05 FCC ID : 2A76ELW-360 APPLICATION PURPOSE : Original Equipment PRODUCT DESIGNATION : Health-nurturing device BRAND NAME : COLLATERAL KING MODEL NAME : LW-360 APPLICANT : Shenzhen Xudonghui Health Management Co., Ltd. DATE OF ISSUE : Jul. 25, 2022 STANDARD(S) TEST PROCEDURE(S) : FCC Part 15.247 REPORT VERSION : V1.0 Attestation of Global Compliance (Shenzhen) Co., Ltd FCC Test Report Report No.: AGC14609220701FE05 Page 2 of 79 REPORT REVISE RECORD Report Version Revise Time Issued Date Valid Version Notes V1.0 / Jul. 25, 2022 Valid Initial Release Report No.: AGC14609220701FE05 Page 3 of 79 TABLE OF CONTENTS 1. VERIFICATION OF CONFORMITY .................................................................................................................. 5 2. GENERAL INFORMATION .............................................................................................................................. 6 2.1. PRODUCT DESCRIPTION ........................................................................................................................ 6 2.2. TABLE OF CARRIER FREQUENCYS ....................................................................................................... 6 2.3. IEEE 802.11N MODULATION SCHEME .................................................................................................... 7 2.4. RELATED SUBMITTAL(S) / GRANT (S) .................................................................................................... 7 2.5. TEST METHODOLOGY ............................................................................................................................. 7 2.6. SPECIAL ACCESSORIES ......................................................................................................................... 7 2.7. EQUIPMENT MODIFICATIONS ................................................................................................................. 7 2.8. ANTENNA REQUIREMENT....................................................................................................................... 8 3. MEASUREMENT UNCERTAINTY ................................................................................................................... 9 4. DESCRIPTION OF TEST MODES ................................................................................................................. 10 5. SYSTEM TEST CONFIGURATION ................................................................................................................ 11 5.1. CONFIGURATION OF EUT SYSTEM ...................................................................................................... 11 5.2. EQUIPMENT USED IN EUT SYSTEM ..................................................................................................... 11 5.3. SUMMARY OF TEST RESULTS .............................................................................................................. 11 6. TEST FACILITY .............................................................................................................................................. 12 7. OUTPUT POWER ........................................................................................................................................... 13 7.1. MEASUREMENT PROCEDURE ............................................................................................................. 13 7.2. TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) .................................................................... 13 7.3. LIMITS AND MEASUREMENT RESULT .................................................................................................. 14 8. BANDWIDTH .................................................................................................................................................. 15 8.1. MEASUREMENT PROCEDURE ............................................................................................................. 15 8.2. TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) .................................................................... 15 8.3. LIMITS AND MEASUREMENT RESULTS ............................................................................................... 16 9. CONDUCTED SPURIOUS EMISSION........................................................................................................... 29 9.1. MEASUREMENT PROCEDURE ............................................................................................................. 29 9.2. TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) .................................................................... 29 9.3. MEASUREMENT EQUIPMENT USEDJN ................................................................................................ 29 9.4. LIMITS AND MEASUREMENT RESULT .................................................................................................. 29 Report No.: AGC14609220701FE05 Page 4 of 79 10. MAXIMUM CONDUCTED OUTPUT POWER SPECTRAL DENSITY ........................................................ 44 10.1 MEASUREMENT PROCEDURE ............................................................................................................ 44 10.2 TEST SET-UP (BLOCK DIAGRAM OF CONFIGURATION) ................................................................... 44 10.3 MEASUREMENT EQUIPMENT USED ................................................................................................... 44 10.4 LIMITS AND MEASUREMENT RESULT ................................................................................................. 44 11. RADIATED EMISSION ................................................................................................................................. 51 11.1. MEASUREMENT PROCEDURE............................................................................................................ 51 11.2. TEST SETUP ............................................................................…
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Report No.: AGC14609220701FE05 Page 62 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11b with data rate 1 2462MHz Antenna Vertical Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 63 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11g with data rate 6 2412MHz Antenna Horizontal Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 64 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11g with data rate 6 2412MHz Antenna Vertical Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 65 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11g with data rate 6 2462MHz Antenna Horizontal Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 66 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11g with data rate 6 2462MHz Antenna Vertical Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 67 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n20 with data rate 6.5 2412MHz Antenna Horizontal Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 68 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n20 with data rate 6.5 2412MHz Antenna Vertical Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 69 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n20 with data rate 6.5 2462MHz Antenna Horizontal Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 70 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n20 with data rate 6.5 2462MHz Antenna Vertical Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 71 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n40 with data rate 13.5 2422MHz Antenna Horizontal Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 72 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n40 with data rate 13.5 2422MHz Antenna Vertical Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 73 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n40 with data rate 13.5 2452MHz Antenna Horizontal Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 74 of 79 EUT Health-nurturing device Model Name LW-360 Temperature 26°C Relative Humidity 60% Pressure 960hPa Test Voltage Normal Voltage Test Mode 802.11n40 with data rate 13.5 2452MHz Antenna Vertical Test Graph for Peak Measurement Test Graph for Average Measurement RESULT: PASS Report No.: AGC14609220701FE05 Page 75 of 79 12. LINE CONDUCTED EMISSION TEST 12.1. LIMITS OF LINE CONDUCTED EMISSION TEST Frequency Maximum RF Line Voltage Q.P (dBμV) Average (dBμV) 150kHz~500kHz 66-56 56-46 500kHz~5MHz 56 46 5MHz~30MHz 60 50 Note: 1. The lower limit shall apply at the transition frequency. 2. The limit decreases linearly with the logarithm of the frequency in the range 0.15 MHz to 0.50 MHz. 12.2. BLOCK DIAGRAM OF LINE CONDUCTED EMISSION TEST EUT & Support Units Report No.: AGC14609220701FE05 Page 76 of 79 12.3. PRELIMINARY PROCEDURE OF LINE CONDUCTED EMISSION TEST 1. The equipment was set up as per the test configuration to simulate typical actual usage per the user’s manual. When the EUT is a tabletop system, a wooden table with a height of 0.8 meters is used and is placed on the ground plane as per ANSI C63.10 (see Test Facility for the dimensions of the ground plane used). When the EUT is a floor-standing equipment, it is placed on the ground plane which has a 3-12 mm non-conductive covering to insulate the EUT from the ground plane. 2. Support equipment, if needed, was placed as per ANSI C63.10. 3. All I/O cables were positioned to simulate typical actual usage as per ANSI C63.10. 4. All support equipment received AC120V/60Hz power from a LISN, if any. 5. The EUT received DC 5V power from adapter which received AC120V/60Hz power from a LISN. 6. The test program was started. Emissions were measured on each current carrying line of the EUT using a spectrum Analyzer / Receiver connected to the LISN powering the EUT. The LISN has two monitoring points: Line 1 (Hot Side) and Line 2 (Neutral Side). Two scans were taken: one with Line 1 connected to Analyzer / Receiver and Line 2 connected to a 50 Ohm load; the second scan had Line 1 connected to a 50 Ohm load and Line 2 connected to the Analyzer / Receiver. 7. Analyzer / …
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Report No.: AGC14609220701AP01 Page 1 of 2 TEST SETUP PHOTOS RADIATED EMISSION TEST SETUP BELOW 1GHz RADIATED EMISSION TEST SETUP ABOVE 1GHz Report No.: AGC14609220701AP01 Page 2 of 2 AC POWER LINE CONDUCTED TEST SETUP RF CONDUCTED TEST SETUP ****************************************End of Report*************************************
| # | Rule Parts | Frequency Range | Power Output |
|---|---|---|---|
| 1 | 15C | 2.41 GHz - 2.46 GHz | 154.90 mW |