ANGIO-PRESS LITE DVT Compression Device— 510(k) K173012

Name: FDA 510(k) clearance K173012
Creator: U.S. Food and Drug Administration
Published: 2018-05-10

Substantially Equivalent

Pegasus Medical Supply, Inc.

FDA 510(k) clearance K173012 for ANGIO-PRESS LITE DVT Compression Device, Substantially Equivalent on 2018-05-10. 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: 2017-09-27
Decision date: 2018-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taoyuan County, TW

Download summary PDF View on FDA.gov ↗

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