K-number	K141476
Device name	WAVELIGHT FS200 LASER SYSTEM
Applicant	Alcon Research, Ltd. Dba Alcon Laboratories, Inc.
Product code	OOE
Device class	Class II
Decision date	Sep 30, 2014
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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WAVELIGHT FS200 LASER SYSTEM

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