# K003732: Braun Precision Sensor, Model BP 2000 Series

- Pathway: 510(k) (Traditional)
- Applicant: Braun GmbH
- Decided: May 16, 2001 after 163 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
No predicates in its family tree.
20 later devices descend from it; 1 cites it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K142917: BP652N (Hem-6300-Z) (2014), 19 descendants of its own
- K182166: Wrist Blood Pressure Monitor Model BP4350 (2018), 10 descendants of its own
- K212115: Arm-type Fully Automatic Digital Blood Pressure Monitor, Wrist-type Fully Automatic Digital Blood Pressure Monitor (2022), 5 descendants of its own
- K160557: Full Automatic (NIBP) Blood Pressure Monitor (2016), 3 descendants of its own
- K230566: Arm-type Fully Automatic Digital Blood Pressure Monitor, Wrist-type Fully Automatic Digital Blood Pressure Monitor (2023), 2 descendants of its own

Source page: https://510kreport.com/device/K003732
Methodology: https://510kreport.com/methodology