# K111141: Bokang Semi-Auto / Automatic / Wrist Digital Blood Pressure Monitor

- Pathway: 510(k) (Abbreviated)
- Applicant: Wenzhou Bokang Instruments Co., Ltd.
- Decided: Feb 21, 2012 after 305 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: 3 generations back to K871718 (1987). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032499: A & D Medical Lifesource UA-704 Digital Blood Pressure Monitors, A&D Engineering, Inc. (2003) Summary page 1.
- K083681: Bioland Blood Pressure Monitor, Bioland Technology, Ltd. (2009) Summary page 1.

## Indications for use
Bokang Digital Blood Pressure Monitor, Model BK6001, Model BK6002 and Model BK6023 are non-invasive blood pressure (NIBP) monitors which use a standard oscillometric measurement method and intend for noninvasive measurement of systolic and diastolic blood pressure and determination of pulse rate by using an inflating cuff which is wrapped around the upper arm or wrist. The device is indicated for use in adults only.

Source page: https://510kreport.com/device/K111141
Methodology: https://510kreport.com/methodology