K-number	K072925
Device name	CANDELA-INOLASE SERENITY PRO PSF SYSTEM
Applicant	Inolase, Ltd.
Product code	GEX
Device class	Class II
Decision date	Jan 10, 2008
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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CANDELA-INOLASE SERENITY PRO PSF SYSTEM

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