K-number	K033354
Device name	FEMTEC LASER MICROKERATOME
Applicant	20/10 Perfect Vision Optische Gerate GmbH
Product code	GEX
Device class	Class II
Decision date	Feb 18, 2004
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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FEMTEC LASER MICROKERATOME

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