# K143202: ANGIO-PRESS DVT Compression Device Model Name: IPCS

- Pathway: 510(k) (Traditional)
- Applicant: Pegasus Medical Supply, Inc.
- Decided: Jul 7, 2015 after 242 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- 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 K101915 (2010). 1 ancestor in all.
1 later device descends from it; 1 cites 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)
- K101915: Vasopress Supreme Mini Model VP500DM, Compression Therapy Concepts, Inc. (2010) Summary page 4.

## Most influential descendants
- K173012: ANGIO-PRESS LITE DVT Compression Device (2018), 0 descendants of its own

## Indications for use
The Pegasus Medical Supply Inc. ANGIO-PRESS IPCS Deep Vein Thrombosis (DVT) Compression Devices are intended to increase venous blood flow in patients in order to help prevent deep vein thrombosis.

Source page: https://510kreport.com/device/K143202
Methodology: https://510kreport.com/methodology