K-number	K013499
Device name	DIOMED 15 PLUS AND DIOMED 30PLUS LASERS
Applicant	Diomed, Inc.
Product code	GEX
Device class	Class II
Decision date	Nov 16, 2001
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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DIOMED 15 PLUS AND DIOMED 30PLUS LASERS

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