K-number	K101601
Device name	AFFIRM DO DIODE LASER
Applicant	Cynosure, Inc.
Product code	GEX
Device class	Class II
Decision date	Sep 23, 2010
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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AFFIRM DO DIODE LASER

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