# K202372: Upper Arm Electronic Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Conmo Electronic Company Limited
- Decided: Dec 30, 2020 after 133 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: 4 generations back to K052153 (2005). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170605: Upper Arm Type Electronic Blood Pressure Monitor Series, Electronic Blood Pressure Monitor: YE650A, YE650D, YE660B, YE670A and YE670D, Jiangsu Yuyue Medical Equipment & Supply Co., Ltd. (2018) Summary page 5.

## Indications for use
Upper Arm Electronic blood pressure monitor is intended to measure the blood pressure and pulse rate of adult at household or medical center. (Not suitable for neonate, pregnancy or pre-eclampsia).

Source page: https://510kreport.com/device/K202372
Methodology: https://510kreport.com/methodology