# K131026: Bosch Blood Pressure Meter (BP5000 BT)

- Pathway: 510(k) (Traditional)
- Applicant: Robert Bosch Healthcare Systems, Inc.
- Decided: Nov 14, 2013 after 216 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: 1 generation back to K050083 (2005). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050083: Blood-Pressure Meter, BPW120, Idt Technology Limited (2005) Summary page 2.

## Indications for use
The Bosch Blood Pressure Monitor (BP5000 BT) is intended for use by adults to measure systolic and diastolic pressures, as well as pulse rate, by the ascillometric method, with a telehealth system or for home use.

Source page: https://510kreport.com/device/K131026
Methodology: https://510kreport.com/methodology