K-number	K013623
Device name	CLEARLIGHT PHOTOTHERAPHY SYSTEM, MODEL CL 420
Applicant	Curelight, Ltd.
Product code	GEX
Device class	Class II
Decision date	Aug 16, 2002
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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CLEARLIGHT PHOTOTHERAPHY SYSTEM, MODEL CL 420

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