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FDA 510(k)

Vas-Q-Clip

K-Number: K151943 · 2016-03-25

Decision Date2016-03-25
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vas-Q-Clip is the device name listed in this FDA 510(k) record. The listed applicant is Nanova Biomaterials, Inc.. It received FDA 510(k) clearance on 2016-03-25 under 510(k) number K151943. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vas-Q-Clip?

Vas-Q-Clip is a medical device that received FDA 510(k) clearance on 2016-03-25. The listed applicant is Nanova Biomaterials, Inc.. The 510(k) number is K151943.

When did Vas-Q-Clip receive FDA 510(k) clearance?

Vas-Q-Clip received FDA 510(k) clearance on 2016-03-25, under 510(k) number K151943.

Who is the listed applicant for Vas-Q-Clip?

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

What is the FDA product code for Vas-Q-Clip?

The FDA product code for Vas-Q-Clip is FZP.

Other records listing Nanova Biomaterials, Inc. as applicant

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.

Related Devices (Code: FZP)

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.

Official Source

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