# K083681: Bioland Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Bioland Technology, Ltd.
- Decided: Jan 16, 2009 after 35 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: 2 generations back to K871718 (1987). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
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.
- K040229: A&D Medical Lifesource Digital Blood Pressure Monitors, Model UB-328, A&D Engineering, Inc. (2004) Summary page 1.
- K040371: A & D Medical UA-767BT Digital Blood Pressure Monitor, A&D Engineering, Inc. (2004) Summary page 1.

## Most influential descendants
- K111141: Bokang Semi-Auto / Automatic / Wrist Digital Blood Pressure Monitor (2012), 0 descendants of its own

## Indications for use
Bioland Blood Pressure Monitor Model 2001, Model 2003, Model 2004, Model 2005, model 3000, Model 3001 and Model 3002, are Sphygmomanometer with Electronic Manometer intended to be used for the indirect (non-invasive) measurement of diastolic, systolic blood pressure and pulse rate for adults only

Source page: https://510kreport.com/device/K083681
Methodology: https://510kreport.com/methodology