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FDA 510(k)

Avulsion Forceps

K-Number: K183428 · 2019-04-16

ApplicantSTERIS Corporation
Decision Date2019-04-16
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Avulsion Forceps is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2019-04-16 under 510(k) number K183428. The device is classified under product code KGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Avulsion Forceps?

Avulsion Forceps is a medical device that received FDA 510(k) clearance on 2019-04-16. The listed applicant is STERIS Corporation. The 510(k) number is K183428.

When did Avulsion Forceps receive FDA 510(k) clearance?

Avulsion Forceps received FDA 510(k) clearance on 2019-04-16, under 510(k) number K183428.

Who is the listed applicant for Avulsion Forceps?

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

What is the FDA product code for Avulsion Forceps?

The FDA product code for Avulsion Forceps is KGE.

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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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