# K233146: Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Jamr Technology Co., Ltd.
- Decided: Mar 19, 2024 after 174 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K251331: Blood Pressure Monitor (B73, BE23T) (2025), 0 descendants of its own

## Indications for use
The Blood Pressure Monitor is intended to measure the systolic and diastolic blood pressure as well as the pulse rate of adult by using the arm cuff (22-42cm), it can be used in medical facilities or at home. It is supplied for OTC use.

Source page: https://510kreport.com/device/K233146
Methodology: https://510kreport.com/methodology