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FDA 510(k)

Bipolar Coagulation Foreceps

K-Number: K210406 · 2021-10-05

ApplicantHangzhou AGS MedTech Co., Ltd.
Decision Date2021-10-05
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Bipolar Coagulation Foreceps is a medical device manufactured by Hangzhou AGS MedTech Co., Ltd.. It received FDA 510(k) clearance on 2021-10-05 under approval number K210406. 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 Bipolar Coagulation Foreceps?

Bipolar Coagulation Foreceps is a medical device that received FDA 510(k) clearance on 2021-10-05. It is manufactured by Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K210406.

When was Bipolar Coagulation Foreceps approved by the FDA?

Bipolar Coagulation Foreceps received FDA 510(k) clearance on 2021-10-05, under approval number K210406.

What company makes Bipolar Coagulation Foreceps?

Bipolar Coagulation Foreceps is manufactured by Hangzhou AGS MedTech Co., Ltd..

What is the FDA product code for Bipolar Coagulation Foreceps?

The FDA product code for Bipolar Coagulation Foreceps is KGE.

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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.

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