# K173012: ANGIO-PRESS LITE DVT Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Pegasus Medical Supply, Inc.
- Decided: May 10, 2018 after 225 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: 2 generations back to K101915 (2010). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143202: ANGIO-PRESS DVT Compression Device Model Name: IPCS, Pegasus Medical Supply, Inc. (2015) Summary page 4.

## Indications for use
The Pegasus Medical Supply Inc. ANGIO-PRESS LITE DVT Compression Device is intended to increase venous blood flow in patients in order to help prevent deep vein thrombosis.

Source page: https://510kreport.com/device/K173012
Methodology: https://510kreport.com/methodology