← Product Code [DXN](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN) · K030230 # AVITA BPM1 SERIES (WRIST TYPE) BLOOD PRESSURE METER (OR MONITOR) (K030230) _Avita Corporation · DXN · May 23, 2003 · Cardiovascular · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN/K030230 ## Device Facts - **Applicant:** Avita Corporation - **Product Code:** [DXN](/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN.md) - **Decision Date:** May 23, 2003 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 870.1130 - **Device Class:** Class 2 - **Review Panel:** Cardiovascular ## Indications for Use AVITA BPM1 Series Wrist Type Blood Pressure Meter is intended to measure the systolic and diastolic blood pressure, and pulse rate(heart rate) by using an inflating cuff which is wrapped around the wrist. The Device is indicated for use by people over 15 years old in home use. ## Device Story Wrist-worn blood pressure monitor; uses inflating cuff to measure systolic/diastolic blood pressure and pulse rate. Designed for home use by individuals over 15 years old. Device captures oscillometric signals via cuff; processes data to calculate blood pressure and heart rate; displays results on integrated LCD panel. Provides patients with self-monitoring capability for blood pressure management. Clinical decision-making supported by providing objective measurements to users. ## Clinical Evidence Comparison study performed against auscultatory method. Clinical repeatability demonstrated to be statistically and clinically acceptable. ## Technological Characteristics Wrist-type non-invasive blood pressure monitor. Conforms to EN-1060-1, EN-1060-3, ANSI/AAMI SP-10, IEC 60601-1, and IEC 60601-1-2. Oscillometric measurement principle. Integrated LCD display. ## 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 - HL-168D Wrist Blood Pressure Monitor ([K012310](/device/K012310.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ 510(K) SUMMARY **MAY 23 2003** (030230 1 of 2 This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA and 21 CFR §807.92 ... | 1.0 | Submitter's Name: | AVITA Corp | |-----|---------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | Address: | 9F, No. 78, Sec. 1, Kwang-Fu Rd., San-Chung, Taipei County,
Taiwan, R.O.C. | | | Phone: | 001-886-2-85121568 | | | Fax: | 001-886-2-85121347 | | | Contact: | Mr. Geo Lin, General Manager | | 2.0 | Device Name: | AVITA BPM1Series (Wrist Type) Blood Pressure Meter (or Monitor)
Model No.: BPM1XY | | | | ► The first Character (blank, 0-9 or A-Z )is for the minor
change revision of device (The Minor change meaning
device change that do not affect the conformity test result of
EMC & Safety, ie. IEC 60601-1 and IEC 60601-1-2 )
► The second Character (blank, 0-9 or A-Z ) is for the color of
the housing
(for example Wellex Blood Pressure Monitor # BPM101, is for
the first revision of device design and the present version of color &
artwork) | | 3.0 | Classification: | Class II | | 4.0 | Predicate Device: | AVITA BPM1 Series Wrist Type Blood Pressure Monitor has
similar general design with HL-168D Wrist Blood Pressure
Monitor(K012310) marketed by Health & Life Co., Ltd.. | | 5.0 | Device Description: | AVITA BPM1 Series Wrist Type Blood Pressure Meter is
designed to measure the systolic and diastolic blood pressure, and
pulse rate(heart of an individual). | | 6.0 | Intended Use: | AVITA BPM1 Series Wrist Type Blood Pressure Meter is
intended to measure the systolic and diastolic blood pressure, and
pulse rate(heart rate) by using an inflating cuff which is wrapped
around the wrist. The Device is indicated for use by people over 15
years old in home use. | {1}------------------------------------------------ ## 7.0 Performance Summary: In terms of operating specification, Safety & EMC requirements, the device conforms to applicable standards included EN-1060-1, EN-1060-3, ANSI/AAMI SP-10, IEC 60601-1 and IEC 60601-1-2 requirements. A comparison study with device that use auscultatory method was performed to validate the performance of the AVITA BPM1 Series Wrist Type Blood Pressure Meter. The comparison study demonstrated that the clinical repeatability of AVITA BPM1 Series Wrist Type Blood Pressure Meter is statistically and clinically acceptable. ## 8. Conclusions: The AVITA BPM1 Series Wrist Type Blood Pressure Meter have the same intended use and similar technological characteristics as HL-168D Wrist Blood Pressure Monitor(K012310) marketed by Health & Life Co., Ltd.. Moreover, bench testing contained in this submission and clinical testing supplied demonstrate that any differences in their technological characteristics do not raise and new questions of safety or effectiveness. Thus, the AVITA BPM1 Series Wrist Type Blood Pressure Meter is substantially equivalent to the predicate devices. {2}------------------------------------------------ Image /page/2/Picture/2 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES · USA" arranged around the perimeter. Inside the circle is a stylized image of a human figure, represented by three overlapping profiles facing to the right, with a bird-like wing extending from the head of the first profile. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 MAY 2 3 2003 AViTA Corporation c/o Ms. Jennifer Reich 3892 South America West Trail Flaggstaff. AZ 86001 Re: K030230 Trade Name: AViTA BPM 1 Series (Wrist type) Blood Pressure Meter (or Monitor) Regulation Number: 21 CFR 870.1130 Regulation Name: Non-Invasive blood measurement system Regulatory Class: Class II (two) Product Code: DXN Dated: April 7, 2003 Received: April 18, 2003 Dear Ms. Reich: 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. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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. 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 {3}------------------------------------------------ Page 2 - Ms. Jennifer Reich 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); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (301) 594-4646. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). 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) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html Sincerely yours, Bram D. Zuckerman, M.D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ K030230 Page _________________________________________________________________________________________________________________________________________________________________________ 510 (k) NUMBER (IF KNOWN): K032230 AVITA BPM1 Series Wrist Type Blood Pressure Meter DEVICE NAME: AVITA Corp. INDICATIONS FOR USE: The device is noninvasive and provide systolic, diastolic blood pressure and pulse rate(heart rate) measurements by using an inflating cuff which is wrapped around the wrist. All values can be read out in one LCD panel. The device is indicated for use by people over 15 years old in home use. (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation | Prescription Use
(Per 21 CFR 801.109) | | |-----------------------------------------------------------|---------| | (Division Sign-Off)
Division of Cardiovascular Devices | | | Over-The-Counter
(Optional Format) | X | | 510(k) Number | K030230 | --- **Source:** [https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN/K030230](https://fda.innolitics.com/submissions/CV/subpart-b%E2%80%94cardiovascular-diagnostic-devices/DXN/K030230) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com