K-number	K090571
Device name	ALMA LASERS ALEX755 MODULE
Applicant	Alma Lasers , Ltd.
Product code	GEX
Device class	Class II
Decision date	Aug 13, 2009
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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ALMA LASERS ALEX755 MODULE

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