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FDA 510(k)

ENDO CLIP III 5MM CLIP APPLIER

K-Number: K121194 · 2012-05-03

ApplicantCovidien
Decision Date2012-05-03
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDO CLIP III 5MM CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2012-05-03 under 510(k) number K121194. 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 ENDO CLIP III 5MM CLIP APPLIER?

ENDO CLIP III 5MM CLIP APPLIER is a medical device that received FDA 510(k) clearance on 2012-05-03. The listed applicant is Covidien. The 510(k) number is K121194.

When did ENDO CLIP III 5MM CLIP APPLIER receive FDA 510(k) clearance?

ENDO CLIP III 5MM CLIP APPLIER received FDA 510(k) clearance on 2012-05-03, under 510(k) number K121194.

Who is the listed applicant for ENDO CLIP III 5MM CLIP APPLIER?

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

What is the FDA product code for ENDO CLIP III 5MM CLIP APPLIER?

The FDA product code for ENDO CLIP III 5MM CLIP APPLIER is 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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