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FDA 510(k)

Vesocclude Polymer Ligating Clip

K-Number: K152082 · 2016-02-26

Decision Date2016-02-26
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Vesocclude Polymer Ligating Clip is the device name listed in this FDA 510(k) record. The listed applicant is Vesocclude Medical, LLC. It received FDA 510(k) clearance on 2016-02-26 under 510(k) number K152082. 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 Vesocclude Polymer Ligating Clip?

Vesocclude Polymer Ligating Clip is a medical device that received FDA 510(k) clearance on 2016-02-26. The listed applicant is Vesocclude Medical, LLC. The 510(k) number is K152082.

When did Vesocclude Polymer Ligating Clip receive FDA 510(k) clearance?

Vesocclude Polymer Ligating Clip received FDA 510(k) clearance on 2016-02-26, under 510(k) number K152082.

Who is the listed applicant for Vesocclude Polymer Ligating Clip?

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

What is the FDA product code for Vesocclude Polymer Ligating Clip?

The FDA product code for Vesocclude Polymer Ligating Clip is FZP.

Related Clinical Trials

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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