K-number	K111303
Device name	DERMATOLOGICAL TREATMENT DEVICE FAMILY
Applicant	Sharplight Technologies, Ltd.
Product code	GEX
Device class	Class II
Decision date	Dec 21, 2011
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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DERMATOLOGICAL TREATMENT DEVICE FAMILY

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