VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30— 510(k) K073028

Substantially Equivalent

Venowave, Inc.

FDA 510(k) clearance K073028 for VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30, Substantially Equivalent on 2008-03-07. Applicant: Venowave, Inc.. Device class: 2.

Clearance details

Applicant
Venowave, Inc.
Product code
Code JOW
Device class
Class 2
Regulation
21 CFR 870.5800
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Stouffville, Ontario, CA
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