K-number	K101990
Device name	ETHICON ENDO-SURGERY GENERATOR G11, MODEL GEN11
Applicant	Ethicon Endo-Sugery, LLC
Product code	GEI
Device class	Class II
Decision date	Jun 13, 2011
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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ETHICON ENDO-SURGERY GENERATOR G11, MODEL GEN11

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