K-number	K901723
Device name	MDL-2000 LASERTRIPTER
Applicant	Candela Laser Corp.
Product code	LNK
Device class	Class II
Decision date	Jul 13, 1990
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MDL-2000 LASERTRIPTER

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