K-number	K043319
Device name	CLAREON AND SOLARUS PULSED LIGHT DEVICES AND ACCESSORIES
Applicant	Novalis Medical, LLC
Product code	GEX
Device class	Class II
Decision date	Dec 17, 2004
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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CLAREON AND SOLARUS PULSED LIGHT DEVICES AND ACCESSORIES

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