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FDA 510(k)

VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30

K-Number: K073028 · 2008-03-07

ApplicantVenowave, Inc.
Decision Date2008-03-07
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30 is the device name listed in this FDA 510(k) record. The listed applicant is Venowave, Inc.. It received FDA 510(k) clearance on 2008-03-07 under 510(k) number K073028. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30?

VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30 is a medical device that received FDA 510(k) clearance on 2008-03-07. The listed applicant is Venowave, Inc.. The 510(k) number is K073028.

When did VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30 receive FDA 510(k) clearance?

VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30 received FDA 510(k) clearance on 2008-03-07, under 510(k) number K073028.

Who is the listed applicant for VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30?

The FDA 510(k) record lists Venowave, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30?

The FDA product code for VENOWAVE MODELS VW5-6, VW5-10, VW5-20 AND VW5-30 is JOW.

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Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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