FDA 510(k)

Vesocclude Polymer Ligating Clip

Número K: K152082 · 2016-02-26

Data da decisão2016-02-26

Código do produtoFZP

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

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