K-number	K101006
Device name	WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
Applicant	Alcon Research, Ltd.
Product code	GEX
Device class	Class II
Decision date	Oct 21, 2010
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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WAVELIGHT FS200 LASER SYSTEM MODEL: FS200

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