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

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..

Clearance details

Applicant: Pegasus Medical Supply, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2017-09-27
Decision date: 2018-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taoyuan County, TW

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