← Product Code [DXN](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN) · K134029 # BELTER BLOOD PRESSURE METER (K134029) _Shenzhen Belter Health Measurement and Analysis TE · DXN · Jul 25, 2014 · Cardiovascular · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN/K134029 ## Device Facts - **Applicant:** Shenzhen Belter Health Measurement and Analysis TE - **Product Code:** [DXN](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN.md) - **Decision Date:** Jul 25, 2014 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 870.1130 - **Device Class:** Class 2 - **Review Panel:** Cardiovascular ## Intended Use Belter Blood pressure meter is intended to measure the systolic and diastolic blood pressure as well as the pulse rate of adult person. It can be used at medical facilities or at home. The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. ## Device Story Belter Blood pressure meter (ePA-46B) is an automated, non-invasive oscillometric device for measuring systolic/diastolic blood pressure and pulse rate in adults. System components include a microprocessor, pressure sensor, pump, deflation control valve, operation keys, and LCD. Powered by four AA alkaline batteries. Device features memory storage for 60 measurements and Bluetooth connectivity for data transfer. During measurement, the device monitors for irregular heartbeats and provides a warning signal alongside readings. Used in clinical or home settings by patients or clinicians. Output is displayed on the LCD, assisting users in tracking blood pressure trends and identifying potential cardiac rhythm irregularities. ## Clinical Evidence Bench testing only. The device demonstrated compliance with recognized consensus standards including IEC 60601-1 (safety), IEC 60601-1-2 (EMC), ANSI/AAMI SP10 (sphygmomanometer performance), and ISO 10993 (biocompatibility). No clinical trial data was required for this 510(k) submission. ## Technological Characteristics Oscillometric measurement principle. Components: microprocessor, pressure sensor, pump, deflation valve, LCD. Power: 4 AA alkaline batteries. Connectivity: Bluetooth. Biocompatibility: ISO 10993-5, -10. Safety/Performance standards: IEC 60601-1, IEC 60601-1-2, ANSI/AAMI SP10, EN1060-1/3/4. Dimensions: 74mm x 152mm x 33mm. Weight: 196g. ## Regulatory Identification A noninvasive blood pressure measurement system is a device that provides a signal from which systolic, diastolic, mean, or any combination of the three pressures can be derived through the use of tranducers placed on the surface of the body. ## Predicate Devices - HEM-7200-Z (BP742) ([K121932](/device/K121932.md)) ## Related Devices - [K181104](/device/K181104.md) — Arm type Blood Pressure Monitor, Digital Blood Pressure Monitor-Automatic Upper Arm Style · Shenzhen Combei Technology Co., Ltd. · Aug 29, 2018 - [K220113](/device/K220113.md) — Upper Arm Electronic Blood Pressure Monitor(Model FC-BP100,FC-BP101,FC-BP102,FC-BP110,FC-BP111,FC-BP112) · Shenzhen Finicare Co., Ltd. · May 31, 2022 - [K172896](/device/K172896.md) — Arm Type Automatic Blood Pressure Monitor BP310A, BP313A, BP351A, BP362A, BP366A, BP369A, BP380A, BP389A, BP-JC312 · Shenzhen Jiacom Technology CO ., Ltd. · Jan 26, 2018 - [K113083](/device/K113083.md) — TRULY AUTOMATIC ARM BLOOD PRESSURE MONITOR · Truly Instrument Co., Ltd. · Jan 19, 2012 - [K242721](/device/K242721.md) — Upper Arm Electronic Blood Pressure Monitor (FC-BP103, FC-BP106, FC-BP113, FC-BP120, FC-BP121, FC-BP130, FC-BP131) · Shenzhen Finicare Co., Ltd. · Oct 4, 2024 ## Submission Summary (Full Text) {0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the word "OBELTER" in a bold, sans-serif font. The letters are black and have a slightly distressed or textured appearance, as if they were printed on a rough surface. The letters are arranged horizontally, with each letter clearly legible despite the textured effect. ## 510(K) Summary JUL 2 5 2014 K134029 #### Date: December 12, 2013 Section 5 #### Submitter Information Name: Shenzhen Belter Health Measurement and Analysis Technology Co.,ltd Address: 702,704, block C ,Tsinghua Unis science park,No.13 Langshan Rd,Hi-Tech Industrial park(north),Nanshan District,518057 shenzhen,People's Republic of China Tel: 0755-61869839 Fax: 0755-61869122 Contact person: pang ming E-mail: pangm@ebelter.com #### Name of device Trade name: Belter Blood pressure meter ,Model: ePA-46B Common name: Belter Blood pressure meter Classification name: System, Measurement, Blood Pressure, Noninvasive Production regulation: 21CFR 870.1130 Product code: DXN #### Predicate Device HEM-7200-Z (BP742)( Omron Healthcare Inc.,DXN,K121932) #### Description The Belter Blood pressure meter can automatically complete the inflation,deflation and measurement .which can measure systolic and diastolic blood pressure as well as the pulse rate of adult person with arm circumference ranging from 22 cm to 36cm by the oscillometric technique. User can select the blood pressure unit mmHg or KPa. The device consists of the microprocessor, pressure sensor, operation keys, pump, deflation control valve and LCD. The subject device is powered by four AA alkaline batteries. The device has a memory function that automatically stores up to 60 sets of the latest measurements. It can also display the latest measurement result. The subject device embeds a Bluetooth that allows it to transport the measurement data to nearby receiving end. The device also detects the appearance of irregular heartbeats during measurement. and gives a warning signal with readings. {1}------------------------------------------------ #### Intended use Belter Blood pressure meter is intended to measure the systolic and diastolic blood pressure as well as the pulse rate of adult person. It can be used at medical facilities or at home. The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. #### Substantially Equivalent The Belter Blood pressure meter (ePA-46B) has the similar essential performance and the same Operation Principle as the predicated devices. | | Belter | Omron | | |------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------| | Compared | ePA-46B | HEM-7200-Z (BP742)<br>(K121932) | | | item | | | | | Indications<br>for Use | Belter Blood pressure<br>meter is intended to<br>measure the systolic and<br>diastolic blood pressure as<br>well as the pulse rate of<br>adult person. It can be<br>used at medical facilities or<br>at home.<br>The device detects the<br>appearance of irregular<br>heartbeats during<br>measurement and gives a<br>warning signal with<br>readings. | The device is a digital<br>monitor intended for use in<br>measuring blood pressure<br>and pulse rate in adult<br>patient population.<br>The device detects the<br>appearance of irregular<br>heartbeats during<br>measurement and gives a<br>warning signal with<br>readings. | Similar | | Intended<br>patient | Adult | Adult | Same | | Environmen<br>t of use | medical facilities or home | Home | Similar | | Operation<br>Principle | Oscillometric | Oscillometric | Same | | Measureme<br>nt Range | Pressure: 0-280mmHg<br>Pulse Rate: 40-200 bpm | Pressure: 0-299mmHg<br>Pulse Rate: 40 -180bpm | Similar | | Accuracy | Pressure : ±3mmHg<br>(±0.4kPa)<br>Pulse Rate: ±5% | Pressure: ±3mmHg<br>(±0.4kPa) or 2%<br>of reading<br>Pulse Rate: ±5% | Similar | | Display<br>screen | LCD | LCD | Same | | Scale<br>Selection | mmHg/Pka | mmHg/Pka | Same | | Cuff | 22-36 cm | 22-46cm | Similar | | Memory | 60sets | 30sets | Similar | | Power<br>supply | 4 AA batteries | 4 AA batteries or AC<br>Adaptor (AC 100-240 V) | Similar | | Operating<br>Environmen<br>t | Temperature : +10°C ~<br>+40°C ; Humidity : 30 ~<br>85%RH | Temperature : +10°C ~<br>+40°C; Humidity : 30 to<br>85%RH | Similar | | Storage<br>Environmen<br>t | Temperature : -20 °C ~<br>+50°C;<br>Humidity: 20%~95% | Temperature : -25 °C ~<br>+60°C;<br>Humidity: 10%~95% | Similar | | Weight | 196g | 340g(Not Including<br>batteries) | Similar | | Size | 74mm×152mm×33mm | 141mm×123mm×85mm | Similar | | Conformanc<br>e standard | IEC 60601-1, IEC<br>60601-1-2, ANSI/AAMI<br>SP10, ISO 10993-5,-10 | IEC 60601-1, IEC<br>60601-1-2, ANSI/AAMI<br>SP10, ISO 10993-5,-10 | Same | Table 1 {2}------------------------------------------------ Image /page/2/Picture/0 description: The image shows the word "BELTER" with a symbol that looks like a lowercase "e" in front of it. The text is in a bold, sans-serif font and appears to be slightly distressed or textured. The color of the text is black, and the background is white. #### Performance Data The following practices were followed and monitored for development of the Belter Blood pressure meter: - IEC 60601-1 Medical Electrical Equipment-Part 1: General Requirements for . Safety, 1988+A1:1991+A2:1995 - . IEC 60601-1-2 Medical Electrical Equipment-Part 1-2: General Requirements for Safety -Collateral Standard: Electromagnetic Compatibility-Requirements and Tests. 2007 - ANSI/AAMISP10 Manual, electronic, or automated sphygmomanometers, . 2002/A1:2003 - Medical electrical equipment --Part 1-11: . IEC60601-1-11 General requirements for basic safety and essential performance -Collateral Standard : Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment,2010 - . ISO 10993-1, Biological evaluation of medical devices-Part 1: Evaluation and testing, 2009 - . ISO 10993-5, Biological evaluation of medical devices-Part 5: Tests for In Vitro cytotoxicity, 2009 - . ISO 10993-10, Biological evaluation of medical devices-Part 10: Tests for irritation and delayed-type hypersensitivity, 2010 - . EN1060-1:A1:1995+A2:2009 Non-invasive sphygmomanometers -Part 1: General requirements,2010 - . EN1060-3 ,Non-invasive sphygmomanometers -Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems,2005 - . EN1060-4 Non-invasive sphygmomanometers - Part 4:Test procedures to determine the overall system accuracy of automated Non-invasive {3}------------------------------------------------ Image /page/3/Picture/0 description: The image shows the word "BELTER" with a circled "c" copyright symbol in front of it. The text is in a bold, sans-serif font and appears to be slightly distressed or weathered. The letters are all capitalized and evenly spaced. The overall impression is that of a logo or brand name. sphygmomanometers,2004 ### Conclusion The Belter Blood pressure meter (ePA-46B) is substantially equivalent to the predicate devices. . {4}------------------------------------------------ Image /page/4/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo features a stylized eagle with three swooping lines representing the bird's wings. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES-USA" is arranged in a circular fashion around the eagle. Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-002 July 25, 2014 ShenZhen Belter Health Measurement and Analysis Technology Co., Ltd Mr. Pang Ming, RA Manager 702,704, block C, Tsinghua Unis Science Park, No. 13 Langshan Rd, Hi-tech industrial park (north), Nanshan District, Shenzhen, Guangdong 518057 People's Republic of China Re: K134029 > Trade/Device Names: Belter Blood Pressure Meter, Model ePA-46B Regulatory Number: 21 CFR 870.1130 Regulation Name: Noninvasive Blood Pressure Measurement System Regulatory Class: Class II (Two) Product Code: DXN Dated: June 17, 2014 Received: June 20, 2014 Dear Mr. Pang: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. {5}------------------------------------------------ Page 2 - Mr. Pang Ming Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Image /page/5/Picture/5 description: The image shows a signature block. The text "Sincerely yours," is at the top of the image. Below that is a signature that appears to say "KOLA". The text "Ken Skodacek for" is at the bottom of the image. Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {6}------------------------------------------------ # :3 = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = = #### Section 4 Indications for Use 510(k) Number: _______________________________________________________________________________________________________________________________________________________________ Device Name: Belter Blood pressure meter Model: ePA-46B Indications for Use Belter Blood pressure meter is intended to measure the systolic and diastolic blood pressure as well as the pulse rate of adult person. It can be used at medical facilities or at home. The device detects the appearance of irregular heartbeats during measurement and gives a warning signal with readings. Prescription Use _____________________________________________________________________________________________________________________________________________________________ AND/OR (Part 21 CFR 801 Sub part D) Over-The-Counter Use __ X _ (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Image /page/6/Picture/12 description: The image shows a logo with the text "KODA" in a stylized font. Below the logo, the text "Ken Skodacek for" is present. The logo features a combination of geometric shapes and letterforms, creating a unique visual identity. The overall design appears to be for a campaign or organization associated with Ken Skodacek. 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