# K913595: DS-240 Ambulatory Blood Pressure Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Koven and Assoc., Inc.
- Decided: Mar 27, 1992 after 227 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K093102: Ambulatory Blood Pressure Monitor, Models FB-270 and DS-270 (2010), 0 descendants of its own
- K955887: Newmed Abp-Lite (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K913595
Methodology: https://510kreport.com/methodology