ANGIO-PRESS DVT Compression Device Model Name: IPCS— 510(k) K143202

Name: FDA 510(k) clearance K143202
Creator: U.S. Food and Drug Administration
Published: 2015-07-07

Substantially Equivalent

Pegasus Medical Supply, Inc.

FDA 510(k) clearance K143202 for ANGIO-PRESS DVT Compression Device Model Name: IPCS, Substantially Equivalent on 2015-07-07. Applicant: Pegasus Medical Supply, Inc.. Device class: 2.

Clearance details

Applicant: Pegasus Medical Supply, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2014-11-07
Decision date: 2015-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taoyuan County, TW

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOW

view all

K261807 — Sequential Circulator (SC-4004-DL, SC-4008-DL)2026-09-11
K254217 — Aerloom2026-08-31
K253555 — Flexitouch® Plus Advanced Pneumatic Compression System2026-07-31
K253386 — DVT Garment2026-06-25
K250242 — Compression Therapy Device (LGT-2202DVT)2026-04-24

More clearances from Pegasus Medical Supply, Inc.

view all

K173012 — ANGIO-PRESS LITE DVT Compression Device2018-05-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.