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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 the device name listed in this FDA 510(k) record. The listed applicant is LeMaitre Vascular, Inc.. It received FDA 510(k) clearance on 2018-03-08 under 510(k) 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. The listed applicant is LeMaitre Vascular, Inc.. The 510(k) number is K173323.

When did AnastoClip GC Closure System receive FDA 510(k) clearance?

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

Who is the listed applicant for AnastoClip GC Closure System?

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

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)

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.

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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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