# K033657: Mobile External Counter Pulsation System Angionew-V

- Pathway: 510(k) (Special)
- Applicant: Living Data Technologies Corporation
- Decided: Dec 19, 2003 after 28 days
- Product code: DRN (Device, Counter-Pulsating, External)
- Device class: 2
- Regulation: 21 CFR 870.5225
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K940264 (1995). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023701: Angionew-IV, Living Data Technologies Corporation (2003) Summary page 1.

## Indications for use
The Mobile External Counter Pulsation System AngioNew-V is a non-invasive external counter pulsating device intended for use in the treatment of patients with congestive heart failure, stable or unstable angina pectoris, actual myocardial infraction or cardiogenic shock.

Source page: https://510kreport.com/device/K033657
Methodology: https://510kreport.com/methodology