K-number	K010192
Device name	ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION
Applicant	Antyllos Medizintechnik GmbH
Product code	GEI
Device class	Class II
Decision date	Apr 2, 2001
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATION

Everything you need for a 510(k) submission. Nothing you don't.