# K030230: Avita BPM1 Series (Wrist Type) Blood Pressure Meter (or Monitor)

- Pathway: 510(k) (Traditional)
- Applicant: Avita Corporation
- Decided: May 23, 2003 after 121 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K012310 (2001). 1 ancestor in all.
8 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012310: Modification to:HL168D Blood Pressure Monitor, Health & Life Co., Ltd. (2001)

## Most influential descendants
- K110299: Digital Automatic Wrist Blood Pressure Monitor WBPM10 Series (2011), 7 descendants of its own
- K120673: Digital Automatic Wrist Blood Pressure Monitor WBPM15 Series (2013), 6 descendants of its own
- K133618: Digital Automatic Wrist Blood Pressure Monitor WBPM22 Series (2014), 5 descendants of its own
- K142088: Digital Automatic Wrist Blood Pressure Monitor SWBPM22 Series (2014), 2 descendants of its own
- K143733: Digital Automatic Wrist Blood Pressure Monitor MD2400 (2015), 1 descendant of its own

## Indications for use
The device is noninvasive and provide systolic, diastolic blood pressure and pulse rateiieart 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.

Source page: https://510kreport.com/device/K030230
Methodology: https://510kreport.com/methodology