K-number	K001093
Device name	CANDELA SPTL-1B PULSED DYE LASER
Applicant	Candela Corp.
Product code	GEX
Device class	Class II
Decision date	Sep 19, 2000
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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CANDELA SPTL-1B PULSED DYE LASER

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