# K151810: Bpump Blood Pressure Cuff

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Pump Medical System Co., Ltd.
- Decided: Dec 17, 2015 after 168 days
- Product code: DXQ (Blood Pressure Cuff)
- Device class: 2
- Regulation: 21 CFR 870.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K010686 (2001). 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)
- K133117: Andon Blood Pressure Cuff, Andon Health Co, Ltd. (2014) Summary page 5.

## Indications for use
The Bpump Blood Pressure Cuff, Model: BC1000, BC8000, are intended to be wrapped on the upper arm and used with a non-invasive blood pressure monitor system to complete the measurement of blood parameters on adults.

Source page: https://510kreport.com/device/K151810
Methodology: https://510kreport.com/methodology