K-number	K880503
Device name	MDL-1 LASERTRIPTER
Applicant	Candela Laser Corp.
Product code	FFK
Device class	Class II
Decision date	Jun 17, 1988
Decision	Substantially Equivalent
Regulation	876.4480

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View the full FDA submission: accessdata.fda.gov

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MDL-1 LASERTRIPTER

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