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 a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2019-04-16 under approval 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. It is manufactured by STERIS Corporation. The 510(k) number is K183428.
When was Avulsion Forceps approved by the FDA?
Avulsion Forceps received FDA 510(k) clearance on 2019-04-16, under approval number K183428.
What company makes Avulsion Forceps?
Avulsion Forceps is manufactured by STERIS Corporation.
What is the FDA product code for Avulsion Forceps?
The FDA product code for Avulsion Forceps is KGE.
Other Devices by STERIS Corporation
Related Devices (Code: KGE)
K161186Fujifilm Diathermic Slitter (FlushKnife), Fujifilm Diathermic Slitter (ClutchCutter)Fujifilm Medical Systems U.S.A, Inc.
K160625Disposable Hot Biopsy ForcepsMicro-Tech (Nanjing) Co., Ltd.
K151474Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)Fujifilm Medical System U.S.A., Inc.
K171916Single Use Hot Biopsy Forceps FD-231Olympus Medical Systems Corp.
K171096Fujifilm Diathermic Slitter (FlushKnife)Fujifilm Medical Systems U.S.A, Inc.
K180018Disposable Hot Biopsy ForcepsMicro-Tech (Nanjing) Co., Ltd.
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.