K-number	K041095
Device name	PHOTOSILK PULSED LIGHT SYSTEM
Applicant	Cynosure, Inc.
Product code	GEX
Device class	Class II
Decision date	May 26, 2004
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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PHOTOSILK PULSED LIGHT SYSTEM

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