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 a medical device manufactured by Vesocclude Medical, LLC. It received FDA 510(k) clearance on 2016-02-26 under approval 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. It is manufactured by Vesocclude Medical, LLC. The 510(k) number is K152082.

When was Vesocclude Polymer Ligating Clip approved by the FDA?

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

What company makes Vesocclude Polymer Ligating Clip?

Vesocclude Polymer Ligating Clip is manufactured by Vesocclude Medical, LLC.

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

NCT06364865 AE05ML Device for ML Hem-o-lok Polymer Clip Delivery in Laparoscopic Surgical Procedures Observational Registery Study COMPLETED

Related Devices (Code: FZP)

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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.