# K012035: Braun Precision Sensor Pro, Model BP 2590

- Pathway: 510(k) (Special)
- Applicant: Braun GmbH
- Decided: Jul 27, 2001 after 28 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.
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 its predicate without a number.
- (no number) Braun PrecisionSensor™ (BP2000 Series) wrist blood pressure monitor: named in the summary without a submission number

## Indications for use
The Braun PrecisionSensor Pro (BP2590) wrist blood pressure monitor is indicated for use for the noninvasive measurement of blood pressure (systolic and diastolic) and pulse rate in adults, in a professional use environment. Use may be initiated as part of a hypertension screening, monitoring, and/or management program supervised by a healthcare provider.

Source page: https://510kreport.com/device/K012035
Methodology: https://510kreport.com/methodology