# K231984: Clinical Automatic Blood Pressure Monitor (DBP-01P,DBP-01HP)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Hingmed Medical Instrument Co., Ltd.
- Decided: Mar 26, 2024 after 265 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: 7 generations back to K982481 (1998). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163683: A&D Medical UA-1200BLE UltraConnect Digital Blood Pressure Monitor, A&D Company, Ltd. (2017) Summary page 5.

## Most influential descendants
- K251307: Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) (2026), 0 descendants of its own

## Indications for use
This device is a digital monitor intended for use in measuring blood pressure(SYS and DIA) and pulse rate ,and the physician reference the result to diagnose. Environments of use: Hospital and other medical establishment. Patient population: Adult (exclude pregnant women ).

Source page: https://510kreport.com/device/K231984
Methodology: https://510kreport.com/methodology