# K142088: Digital Automatic Wrist Blood Pressure Monitor SWBPM22 Series

- Pathway: 510(k) (Traditional)
- Applicant: Grandway Technology (Shenzhen) Limited
- Decided: Oct 31, 2014 after 91 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: 5 generations back to K012310 (2001). 5 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133618: Digital Automatic Wrist Blood Pressure Monitor WBPM22 Series, Grandway Technology (Shenzhen) Limited (2014) Summary page 4.

## Most influential descendants
- K163113: Digital Automatic Wrist Blood Pressure Monitor SWBPM22 Series (2017), 0 descendants of its own
- K151587: Digital Automatic Wrist Blood Pressure Monitor MD3200 (2015), 0 descendants of its own

## Indications for use
This device is for use by medical professional or home users. It is intended to measure the systolic and diastolic blood pressure of an adult individual by using a non-invasive technique, in which an inflatable cuff is wrapped around the wrist.

Source page: https://510kreport.com/device/K142088
Methodology: https://510kreport.com/methodology