K-number	K103667
Device name	SAPPHIRE ST PORTABLE DIODE LASER
Applicant	Den-Mat Holdings, LLC
Product code	GEX
Device class	Class II
Decision date	Dec 29, 2010
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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SAPPHIRE ST PORTABLE DIODE LASER

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