K-number	K210406
Device name	Bipolar Coagulation Foreceps
Applicant	Hangzhou AGS MedTech Co., Ltd.
Product code	KGE
Device class	Class II
Decision date	Oct 5, 2021
Decision	Substantially Equivalent
Regulation	876.4300

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View the full FDA submission: accessdata.fda.gov

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Bipolar Coagulation Foreceps

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