# K023701: Angionew-IV

- Pathway: 510(k) (Traditional)
- Applicant: Living Data Technologies Corporation
- Decided: Jan 30, 2003 after 87 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: 2 generations back to K940264 (1995). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K940264: Vasogenics Eecp-MC2, Vasogenics, Inc. (1995) Summary page 1.
- K020857: Eecp Therapy System Model TS3 with Pulse Oximetry and Enhanced External Counterpulsation Eecp MC-2 External Counter, Vasomedical, Inc. (2002) Summary page 1.
- K012141: Aecp-a, Automatic External Counterpulsation Device, External Counterpulsation Lab (2001) Summary page 1.

## Most influential descendants
- K033657: Mobile External Counter Pulsation System Angionew-V (2003), 0 descendants of its own

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

Source page: https://510kreport.com/device/K023701
Methodology: https://510kreport.com/methodology