K-number	K140732
Device name	CANDELA GENTLELASE FAMILY OF LASER SYSTEMS
Applicant	Candela Corp.
Product code	GEX
Device class	Class II
Decision date	Nov 7, 2014
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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CANDELA GENTLELASE FAMILY OF LASER SYSTEMS

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