K-number	K013493
Device name	INDIGO OPTIMA LASER SYSTEM
Applicant	Ethicon Endo-Surgery, Inc.
Product code	GEX
Device class	Class II
Decision date	Dec 13, 2001
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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INDIGO OPTIMA LASER SYSTEM

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