# K122810: Compact Digital Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Thermor, Ltd.
- Decided: Feb 8, 2013 after 148 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 K061279 (2006). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061279: LD-578 Fully Automatic Digital Blood Pressure Monitor, Little Doctor (Shanghai) Electronic (2006) Summary page 2.

## Indications for use
The Compact Blood Pressure Monitor is intended to measure the systolic, diastolic and pulse rate of an adult individual by using a non-invasive technique in which an inflatable cuff is wrapped around the upper arm. The device is reusable and intended for home use on adults.

Source page: https://510kreport.com/device/K122810
Methodology: https://510kreport.com/methodology