# K093013: Blood Pressure Monitor, Model MD200A

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Choice Electronic Technololgy Co., Ltd.
- Decided: Jan 8, 2010 after 101 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 K903134 (1991). 11 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082881: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model Watchbp O3, Microlife Intellectual Property GmbH (2008) Summary page 1.

## Most influential descendants
- K130056: Patient Monitor (2013), 0 descendants of its own
- K110775: Electronic Sphygmomanometer (2011), 0 descendants of its own
- K110774: Electronic Sphygmomanometer (2011), 0 descendants of its own

## Indications for use
MD200A Blood Pressure Monitor is an automatic electronic blood pressure monitor intended to measure the systolic, diastolic and mean blood pressure as well as pulse rate via non-invasive oscillometric technique in which an inflatable cuff is wrapped around the upper arm. It can be used on adult, pediatric and neonatal individuals.

Source page: https://510kreport.com/device/K093013
Methodology: https://510kreport.com/methodology