K-number	K981090
Device name	LASERLITE DIODE SURGICAL LASER
Applicant	Laserlite, LLC
Product code	GEX
Device class	Class II
Decision date	Apr 21, 1998
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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LASERLITE DIODE SURGICAL LASER

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