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FDA 510(k)

ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02

K-Number: K032896 · 2004-03-17

ApplicantAnson Medical , Ltd.
Decision Date2004-03-17
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02 is the device name listed in this FDA 510(k) record. The listed applicant is Anson Medical , Ltd.. It received FDA 510(k) clearance on 2004-03-17 under 510(k) number K032896. 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 ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02?

ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02 is a medical device that received FDA 510(k) clearance on 2004-03-17. The listed applicant is Anson Medical , Ltd.. The 510(k) number is K032896.

When did ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02 receive FDA 510(k) clearance?

ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02 received FDA 510(k) clearance on 2004-03-17, under 510(k) number K032896.

Who is the listed applicant for ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02?

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

What is the FDA product code for ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02?

The FDA product code for ANSON REFIX VASCULAR AND TISSUE CLIP, MODELS GF-04-01 AND GF-04-02 is 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.

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