WIZAIR DVT— 510(k) K012994

Name: FDA 510(k) clearance K012994
Creator: U.S. Food and Drug Administration
Published: 2002-03-27

Substantially Equivalent

Medical Compression Systems (Dbn) , Ltd.

FDA 510(k) clearance K012994 for WIZAIR DVT, Substantially Equivalent on 2002-03-27. Applicant: Medical Compression Systems (Dbn) , Ltd.. Device class: 2.

Clearance details

Applicant: Medical Compression Systems (Dbn) , Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2001-09-06
Decision date: 2002-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ra'Ananna 43373, IL

Download summary PDF View on FDA.gov ↗

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