K-number	K041957
Device name	EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
Applicant	Diomed, Inc.
Product code	GEX
Device class	Class II
Decision date	Dec 1, 2004
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS

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