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F6O-INBODY-BP170BBlood Pressure Monitor

InBody Co., Ltd.
Blood Pressure Monitor - FCC ID F6O-INBODY-BP170B - InBody Co., Ltd.
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Application Details

Equipment Class
DTS - Digital Transmission System
Date of Grant
Aug 19, 2020
Application Purpose
Original Equipment
Date of Application
Aug 19, 2020
Equipment Note
Blood Pressure Monitor
Frequency Range
2402.00000000 - 2480.00000000
Company
InBody Co., Ltd.
Country
South Korea

Documents & Files

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Users Manual

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Cover Letter(s)

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External Photos

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ID Label/Location Info

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Internal Photos

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RF Exposure Info

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Test Report

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Test Setup Photos

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Document Text

Text extracted from the exhibit documents filed with the FCC. Open a document above to read the original.

Users Manual

User’s Manual BP170 / BP170B Automatic Blood Pressure Monitor ©2020 InBody Co., Ltd. All rights reserved. BM-ENG-L5-C-200222 Please note the important information below before reading this manual. InBody Co., Ltd. [HEAD OFFICE] 625, InBody Bldg., Eonju-ro, Gangnam-gu, Seoul 06106 Republic of Korea TEL: +82-2-501-3939 FAX: +82-2-578-5669 Website: inbody.com E-mail: [email protected] ©2020 InBody Co., Ltd. All rights reserved. Reproduction, adaptation, or translation of this manual is prohibited without prior written consent from InBody Co., Ltd. under the copyright laws. This manual may be printed incorrectly and subject to change without notice. InBody Co., Ltd. shall not be liable for any errors, incidental, or consequential damages that occurred by not complying with the content of the User ̓s Manual. Visit our website (inbody.com) to view and download additional information about the BP170(B). InBody Co.,Ltd. reserves the right to modify the appearance, specifications, etc. of this product to improve its quality, without prior notice. Failure to observe these precautions can result in personal injury or equipment damage. Warning Caution Failure to comply with safety precautions can damage the equipment. Note Referring to notes can help improve equipment use. InBody Co., Ltd. [HEAD OFFICE] InBody Europe B.V. Gyroscoopweg 122, 1042 AZ, Amsterdam, The Netherlands TEL: +31-20-238-6080 FAX: +31-6-5734-1858 Website: nl.inbody.com E-mail: [email protected] Australian Sponsor. [AUSTRALIA] Emergo AUSTRALIA. Level 20, Tower II, Darling Park, 201 Sussex Street, Sydney, NSW 2000, AUSTRALIA TEL: +61-2-9006-1662 FAX: +61-2-9006-1010 Website: emergogroup.com E-mail: [email protected] Customer Service Information InBody USA [USA] 13850 Cerritos Corporate Dr. Unit C Cerritos, CA 90703 USA TEL: +1-323-932-6503 FAX: +1-323-952-5009 Website: inbody.com E-mail: [email protected] InBody Japan [JAPAN] Tani Bldg., 1-28-6, Kameido, Koto-ku, Tokyo 136-0071 Japan TEL: +81-3-5875-5780 FAX: +81-3-5875-5781 Website: inbody.co.jp E-mail: [email protected] InBody China [CHINA] 904, XingDiPlaza, No.1698 YiShanRoad, Shanghai 201103 China TEL: +86-21-64439705 FAX: +86-21-64439706 Website: inbodychina.com E-mail: [email protected] InBody India [INDIA] Unit No. G-B 10, Ground Floor, Art Guild House, Phoenix Market City, L.B.S. Marg, Kurla (West), Mumbai 400070 India TEL: +91 22-6223-1911 Website: inbody.in E-mail: [email protected] InBody Asia [ASIA] Unit 3A-11, Oval Damansara, 685 Jalan Damansara Kuala Lumpur, WP KL 60000 Malaysia TEL: +60-3-7732-0790 FAX: +60-3-7733-0790 Website: inbodyasia.com E-mail: [email protected] 1. Introduction for BP170(B) 2. Operating BP170(B) A. Preparation for Measurement B. Blood Pressure Measurement C. Saving Measurement Results D. Check the Stored Blood Pressure 3. Storage 4. Frequently Asked Questions (FAQ) A. Regarding the Measurement B. Regarding Error 5. Others A. Safety Information B. Optional Equipment C. Safety Information D. Classification E. Specifications Warranty 6 8 11 15 16 17 18 21 22 26 26 27 27 User’s Manual Contents BP170 / BP170B Automatic Blood Pressure Monitor 1. Introduction for BP170(B) InBody BP170(B) is a compact and easy-to-use automatic blood pressure monitor. BP170(B) uses an oscillometric method and adopts downward exhaust type, which measures blood pressure by exhausting air from the pressurized cuff. Main users are ordinary people who need regular blood pressure management. * Product Components ❶ Main Body (1EA) ❷ Cuff (1EA) ❸ AA Size Alkaline Batteries (4EA) ❹ User ̓s Manual (1EA) ❺ Storage Pouch (1EA) ❻ Dedicated AC Adaptor (Optional) * Names of Main Unit Parts Storing Button 1 Decrease Button Storing Button 2 Cuff connection Increase Button Start / Stop Button AC adaptor connection Rear mount Battery tray ❶ ❷ ❸ ❹ ❺ ❻ 7 * Names of Cuff Parts Checking mark for the available arm circumference Wearing location mark Air inlet (Connection with main body) Air tube * Display Screen Parts Name Faulty in cuff worn state Blood pressure state display Time Remaining battery indicator Mute Bluetooth connection (Option for BP170B only) AC adaptor connection indicator Normal in cuff worn state Systolic Blood Pressure Date Diastolic Blood Pressure Storing location 1 Storing location 2 Average blood pressure Heartbeat detection Pulse Rate Manual Pressurization Morning Surge Hypertension detection Irregular heartbeat detection Movement detection 8 2. Operating BP170(B) A. Preparation for Measurement * If BP170(B) has been stored in a hot or cold environment, keep it in a room temperature for at least one hour. (1) Inserting / replacing the batteries ❶ Remove the battery cover. ❷ Insert four(4) AA size batteries in the correct direction. ❸ Close the battery cover. • Be careful with the polarity + and - of the batteries during insertion. • Dispose the used batteries only in designated location. • Use 1.5V AA-size alkaline or manganese batteries. • Use all four(4) batteries of the same company and same model in the time of replacement. Cautions - - - : The capacity of the batteries is sufficient. : The batteries are soon be exhausted. : The batteries have been completely exhausted. Please replace with new batteries. (2) Remaining battery indicator - User may check the remaining battery level in the upper right corner of the screen while BP170(B) is in use. - Battery level is not displayed when the AC adapter is used. Instead, AC adapter icon ( ) appears. Instead, AC adapter icon ( ) appears. 9 (3) Use of the dedicated AC adaptor (Optional) ❶ Connect the dedicated AC adapter plug to the main body of BP170(B). ❷ Connect the dedicated AC adaptor to the outlet. • When disconnecting the AC adapter, disconnect the AC adapter from the outlet first, and then disconnect the AC adapter from the main body of BP170(B). Caution ❶ ❷ (4) Mute Press and buttons at the same time and hold for 2-3 seconds to turn off the sound. BP170(B) should be turned off when doing so. Mute Icon 1…

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Cover Letter(s)

Date: August 6, 2020 Office of Engineering Technology Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 RE: New Family Listing Declaration Please review the attached exhibits supporting our request for applying New Family Listing to the FCC ID: F6O-INBODY-BP170B for Company Name: InBody Co., Ltd. Product Description: Blood Pressure Monitor Base model: BP170B Additional model(s): BP160B The only difference between the base model BP170B and the additional model(s) BP160B is as follows: Model Name Differences BP170B Basic Model (One-touch Cuff) BP160B The models are identical to basic model but the Cuff is different. (Normal Cuff) BP170B(One-touch Cuff) BP160B(Normal Cuff) Should you have any questions, please contact us. Sincerely, Name: Kyung Keun, Kim Title: Manager

Cover Letter(s)

Letter of Authorization Company : InBody Co., Ltd. Address : InBody Bldg., 625, Eonju-ro, Gangnam-gu, Seoul, 06106, South Korea Product Name : Blood Pressure Monitor Model Number : BP170B FCC Identifier : F6O-INBODY-BP170B We authorize MiCOM Labs Inc, 575 Boulder Court, Pleasanton, California 94566, USA, to act on our behalf on all matters concerning the above named equipment. Any individual within MiCOM Labs is authorized to act on our behalf and take action on the application. We declare that MiCOM Labs Inc, 575 Boulder Court, Pleasanton, California 94566, USA, is allowed to forward all information related to the approval project to the Federal Communication Commission 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. Name: Kyung Keun, Kim Date: August 6, 2020 Title: Manager Signature of applicant:

Cover Letter(s)

Office of Engineering Technology Federal Communications Commission 7435 Oakland Mills Road Columbia, MD 21046 Date: August 6, 2020 Subject; Request for Confidentiality FCC ID: F6O-INBODY-BP170B To Whom It May Concern, Pursuant to the provisions of Sections 0.457 and 0.459 of Commission's rules (47CFR0.457, 0.459), we are requesting the Commission to withhold the following attachment(s) as confidential document from public disclosure indefinitely. • Schematic Diagram • Block Diagram • Part List • Operational Description Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. In additional to above mentioned documents, pursuant to Public Notice DA 04-1705 of the Commission' s policy, in order to comply with the marketing regulations in 47 CFT §2.803 and the importation rules in 47 CFR §2.1204, while ensuring that business sensitive information remains confidential until the actual marketing of newly authorized devices. We are requesting the commission to grant shot-term confidentiality request on the following attachment(s) for 180 days after the grant as outlined in Public Notice DA 04-1705. • External Photos • Internal Photos • Test Setup Photos • User Manual It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and those information will be available for public review once the grant of equipment authorization is issued. Sincerely, Name: Kyung Keun, Kim Title: Manager

External Photos

Page 1 of 6 Page 2 of 6 Page 3 of 6 Page 4 of 6 Page 5 of 6 Page 6 of 6

ID Label/Location Info

Page 1 of 1 IDENTIFICATION LABEL: PROPOSED LABEL The shall be permanently affixed in the rear side of the equipment

Internal Photos

Page 1 of 8 Page 2 of 8 Page 3 of 8 Page 4 of 8 Page 5 of 8 Page 6 of 8 Page 7 of 8 Page 8 of 8 Chip Antenna

RF Exposure Info

Page 1 of 7 Report No.: OT-207-RWD-063 It should not be reproduced except in full, without the written approval of ONETECH Corp. EMC-003 (Rev.2) ONETECH Corp.: 43-14, Jinsaegol-gil, Chowol-eup, Gwangju-si, Gyeonggi-do, 12735, Korea (TEL: 82-31-799-9500, FAX: 82-31-799-9599) ELECTROMAGNETIC EMISSION COMPLIANCE REPORT FOR LOW-POWER, NON-LICENSED TRANSMITTER Test Report No. : OT-207-RWD-063 AGR No. : A206A-120 Applicant : InBody Co., Ltd. Address : InBody Bldg., 625, Eonju-ro, Gangnam-gu, Seoul, 06106, South Korea Manufacturer : InBody Co., Ltd. Address : 15, Heugam-gil, Ipjang-myeon, Seobuk-gu, Cheonan-si, Chungcheongnam-do 31025 KOREA Type of Equipment : Blood Pressure Monitor FCC ID. : F6O-INBODY-BP170B Model Name : BP170B Multiple Model Name : BP160B Serial number : N/A Total page of Report : 7 pages (including this page) Date of Incoming : July 08, 2020 Date of issue : July 30, 2020 SUMMARY The equipment complies with the regulation; FCC PART 15 SUBPART C Section 15.247 This test report only contains the result of a single test of the sample supplied for the examination. It is not a generally valid assessment of the features of the respective products of the mass-production. Reviewed by: Approved by: Tae-Ho, Kim / Senior Manager Ki-Hong, Nam / General Manager ONETECH Corp. ONETECH Corp. Page 2 of 7 Report No.: OT-207-RWD-063 It should not be reproduced except in full, without the written approval of ONETECH Corp. EMC-003 (Rev.2) ONETECH Corp.: 43-14, Jinsaegol-gil, Chowol-eup, Gwangju-si, Gyeonggi-do, 12735, Korea (TEL: 82-31-799-9500, FAX: 82-31-799-9599) CONTENTS PAGE 1. VERIFICATION OF COMPLIANCE ............................................................................................................................. 4 2. GENERAL INFORMATION ............................................................................................................................................ 5 2.1 PRODUCT DESCRIPTION ................................................................................................................................................. 5 2.2 ALTERNATIVE TYPE(S)/MODEL(S); ALSO COVERED BY THIS TEST REPORT. ................................................................ 5 3. EUT MODIFICATIONS .................................................................................................................................................... 5 4. MAXIMUM PERMISSIBLE EXPOSURE ...................................................................................................................... 6 4.1 APPLICABLE STANDARD ................................................................................................................................................ 6 4.2 EUT DESCRIPTION ......................................................................................................................................................... 6 4.3 TEST RESULT ................................................................................................................................................................. 7 Page 3 of 7 Report No.: OT-207-RWD-063 It should not be reproduced except in full, without the written approval of ONETECH Corp. EMC-003 (Rev.2) ONETECH Corp.: 43-14, Jinsaegol-gil, Chowol-eup, Gwangju-si, Gyeonggi-do, 12735, Korea (TEL: 82-31-799-9500, FAX: 82-31-799-9599) Revision History Rev. No. Issue Report No. Issued Date Revisions Section Affected 0 OT-207-RWD-063 July 30, 2020 Initial Release All Page 4 of 7 Report No.: OT-207-RWD-063 It should not be reproduced except in full, without the written approval of ONETECH Corp. EMC-003 (Rev.2) ONETECH Corp.: 43-14, Jinsaegol-gil, Chowol-eup, Gwangju-si, Gyeonggi-do, 12735, Korea (TEL: 82-31-799-9500, FAX: 82-31-799-9599) 1. VERIFICATION OF COMPLIANCE Applicant : InBody Co., Ltd. Address : InBody Bldg., 625, Eonju-ro, Gangnam-gu, Seoul, 06106, South Korea Contact Person : Kyung Keun, Kim / Manager Telephone No. : +82-2-300-2241 FCC ID : F6O-INBODY-BP170B Model Name : BP170B Brand Name : Serial Number : N/A Date : July 30, 2020 EQUIPMENT CLASS DTS – DIGITAL TRNSMISSION SYSTEM E.U.T. DESCRIPTION Blood Pressure Monitor THIS REPORT CONCERNS Original Grant MEASUREMENT PROCEDURES ANSI C63.10: 2013 TYPE OF EQUIPMENT TESTED Pre-Production KIND OF EQUIPMENT AUTHORIZATION REQUESTED Certification EQUIPMENT WILL BE OPERATED UNDER FCC RULES PART(S) FCC PART 15 SUBPART C Section 15.247 KDB 558074 D01 15.247 Meas Guidance v05r02 Modifications on the Equipment to Achieve Compliance None Final Test was Conducted On 3 m Semi Anechoic Chamber -. The above equipment was tested by ONETECH Corp. for compliance with the requirement set forth in the FCC Rules and Regulations. This said equipment in the configuration described in this report, shows the maximum emission levels emanating from equipment are within the compliance requirements. Page 5 of 7 Report No.: OT-207-RWD-063 It should not be reproduced except in full, without the written approval of ONETECH Corp. EMC-003 (Rev.2) ONETECH Corp.: 43-14, Jinsaegol-gil, Chowol-eup, Gwangju-si, Gyeonggi-do, 12735, Korea (TEL: 82-31-799-9500, FAX: 82-31-799-9599) 2. GENERAL INFORMATION 2.1 Product Description The InBody Co., Ltd., Model BP170B (referred to as the EUT in this report) is a Blood Pressure Monitor. The product specification described herein was obtained from product data sheet or user’s manual. Device Type Blood Pressure Monitor Temperature Range 10 °C ~ 40 °C Operating Frequency 2 402 MHz ~ 2 480 MHz RF Output Power -7.08 dBm Number of Channel 40 Channel Modulation Type GFSK (Bluetooth LE) Antenna Type Chip Antenna Antenna Gain 1.99 dBi List of each Osc. or crystal Freq.(Freq. >= 1 MHz) 16 MHz 2.2 Alternative type(s)/model(s); also covered by this test report. -. The following lists consist of the added model and their differences. Model Name Differences Tested BP170B Basic Model (One-touch Cuff)  BP160B The models are identical to basic model but the Cuff is different. (Normal…

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Test Report

Page 1 of 39 Report No.: OT-207-RWD-062 It should not be reproduced except in full, without the written approval of ONETECH Corp. EMC-003 (Rev.2) ONETECH Corp.: 43-14, Jinsaegol-gil, Chowol-eup, Gwangju-si, Gyeonggi-do, 12735, Korea (TEL: 82-31-799-9500, FAX: 82-31-799-9599) ELECTROMAGNETIC EMISSION COMPLIANCE REPORT FOR LOW-POWER, NON-LICENSED TRANSMITTER Test Report No. : OT-207-RWD-062 AGR No. : A206A-120 Applicant : InBody Co., Ltd. Address : InBody Bldg., 625, Eonju-ro, Gangnam-gu, Seoul, 06106, South Korea Manufacturer : InBody Co., Ltd. Address : 15, Heugam-gil, Ipjang-myeon, Seobuk-gu, Cheonan-si, Chungcheongnam-do 31025 KOREA Type of Equipment : Blood Pressure Monitor FCC ID. : F6O-INBODY-BP170B Model Name : BP170B Multiple Model Name : BP160B Serial number : N/A Total page of Report : 39 pages (including this page) Date of Incoming : July 08, 2020 Date of issue : July 30, 2020 SUMMARY The equipment complies with the regulation; FCC PART 15 SUBPART C Section 15.247 This test report only contains the result of a single test of the sample supplied for the examination. It is not a generally valid assessment of the features of the respective products of the mass-production. Reviewed by: Approved by: Tae-Ho, Kim / Senior Manager Ki-Hong, Nam / General Manager ONETECH Corp. ONETECH Corp. Page 2 of 39 Report No.: OT-207-RWD-062 It should not be reproduced except in full, without the written approval of ONETECH Corp. EMC-003 (Rev.2) ONETECH Corp.: 43-14, Jinsaegol-gil, Chowol-eup, Gwangju-si, Gyeonggi-do, 12735, Korea (TEL: 82-31-799-9500, FAX: 82-31-799-9599) CONTENTS PAGE 1. VERIFICATION OF COMPLIANCE ............................................................................................................................. 5 2. TEST SUMMARY .............................................................................................................................................................. 6 2.1 TEST ITEMS AND RESULTS ............................................................................................................................................. 6 2.2 ADDITIONS, DEVIATIONS, EXCLUSIONS FROM STANDARDS ........................................................................................... 6 2.3 RELATED SUBMITTAL(S) / GRANT(S) ............................................................................................................................ 6 2.4 PURPOSE OF THE TEST ................................................................................................................................................... 6 2.5 TEST METHODOLOGY .................................................................................................................................................... 6 2.6 TEST FACILITY ............................................................................................................................................................... 6 3. GENERAL INFORMATION ............................................................................................................................................ 7 3.1 PRODUCT DESCRIPTION ................................................................................................................................................. 7 3.2 ALTERNATIVE TYPE(S)/MODEL(S); ALSO COVERED BY THIS TEST REPORT. ................................................................ 7 4. EUT MODIFICATIONS .................................................................................................................................................... 7 5. SYSTEM TEST CONFIGURATION ............................................................................................................................... 8 5.1 JUSTIFICATION ............................................................................................................................................................... 8 5.2 PERIPHERAL EQUIPMENT .............................................................................................................................................. 8 5.3 MODE OF OPERATION DURING THE TEST ...................................................................................................................... 8 5.4 CONFIGURATION OF TEST SYSTEM ............................................................................................................................. 10 5.5 ANTENNA REQUIREMENT ............................................................................................................................................ 10 6. PRELIMINARY TEST .................................................................................................................................................... 10 6.1 AC POWER LINE CONDUCTED EMISSIONS TESTS ....................................................................................................... 10 6.2 GENERAL RADIATED EMISSIONS TESTS ..................................................................................................................... 10 7. MINIMUM 6 DB BANDWIDTH .................................................................................................................................... 11 7.1 OPERATING ENVIRONMENT ......................................................................................................................................... 11 7.2 TEST SET-UP ................................................................................................................................................................. 11 7.3 TEST EQUIPMENT USED ................................................................................................................................................ 11 7.4 TEST DATA .................................................................................................................................................................... 12 8. MAXIMUM PEAK OUTPUT POWER .......................................…

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Test Setup Photos

Page 1 of 5 - Conducted Emission Test Page 2 of 5 - Radiated Emission Test -. BATTERY Mode Page 3 of 5 Page 4 of 5 -. ADAPTER Mode Page 5 of 5

Contact Information

Applicant

Min seok Lee(Manager)
[email protected]+82-02-2182-8918Fax: +82-02-578-5669

Technical Contact

InBody Co., Ltd.
[email protected]

South Korea

Test Firm

ONETECH Corp.Ki Hong Nam
[email protected]82-31-799-9580Fax: 82-31-799-9599

Technical Specifications

#Rule PartsFrequency RangePower Output
115C2.40 GHz - 2.48 GHz200.00 µW
Confidentiality
Long Term
Grant Notes
Power listed is the maximum conducted output power .

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