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FDA 510(k)

AnastoClip GC Closure System

K-Number: K173323 · 2018-03-08

ApplicantLeMaitre Vascular, Inc.
Decision Date2018-03-08
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AnastoClip GC Closure System is a medical device manufactured by LeMaitre Vascular, Inc.. It received FDA 510(k) clearance on 2018-03-08 under approval number K173323. 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 AnastoClip GC Closure System?

AnastoClip GC Closure System is a medical device that received FDA 510(k) clearance on 2018-03-08. It is manufactured by LeMaitre Vascular, Inc.. The 510(k) number is K173323.

When was AnastoClip GC Closure System approved by the FDA?

AnastoClip GC Closure System received FDA 510(k) clearance on 2018-03-08, under approval number K173323.

What company makes AnastoClip GC Closure System?

AnastoClip GC Closure System is manufactured by LeMaitre Vascular, Inc..

What is the FDA product code for AnastoClip GC Closure System?

The FDA product code for AnastoClip GC Closure System is FZP.

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Related Devices (Code: FZP)

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Official Source

View on FDA Database →

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

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