# K083466: MD2000A Vital Sign Monitor, Model MD2000A

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Choice Electronic Technololgy Co., Ltd.
- Decided: Apr 3, 2009 after 130 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The MD2000.A vital sign monitor is portable device indicated for use in non-invasively measuring and displaying functional oxygen saturation of arterial haemoglobin (SpO2), and pulse rate of adult, pediatric and neonate patients via finger in hospitals, medical fdcilities, and subacute environments. The vital sign monitor is intended' for spot-checking and/or continuous monitoring of patients, the sensor of device is reusable..

Source page: https://510kreport.com/device/K083466
Methodology: https://510kreport.com/methodology