K-number	K062314
Device name	HORUS LASER KERATOME
Applicant	Carl Zeiss Meditec, AG
Product code	GEX
Device class	Class II
Decision date	Dec 22, 2006
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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HORUS LASER KERATOME

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