K-number	K072034
Device name	DIODE MEDICAL LASER FAMILY, MODELS 4, 6, 30
Applicant	Quanta System Spa
Product code	GEX
Device class	Class II
Decision date	Sep 20, 2007
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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DIODE MEDICAL LASER FAMILY, MODELS 4, 6, 30

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