# K955887: Newmed Abp-Lite

- Pathway: 510(k) (Traditional)
- Applicant: Newmed Corp.
- Decided: Sep 5, 1996 after 252 days
- Product code: DXW (System, Phonocatheter, Intracavitary)
- Device class: 2
- Regulation: 21 CFR 870.1270
- 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 K913595 (1992). 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)
- K913595: DS-240 Ambulatory Blood Pressure Monitoring System, Koven and Assoc., Inc. (1992) Summary page 1.

## Indications for use
The intended use of the ABP-/ite is to detect, diagnose, and monitor hypertension.

Source page: https://510kreport.com/device/K955887
Methodology: https://510kreport.com/methodology