K-number	K081704
Device name	SELECTA FAMILY OF OPHITHALMIC LASER SYSTEMS
Applicant	Lumenis, Inc.
Product code	GEX
Device class	Class II
Decision date	Sep 11, 2008
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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SELECTA FAMILY OF OPHITHALMIC LASER SYSTEMS

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