K-number	K012398
Device name	DIOMED 15 DIODE LASER
Applicant	Diomed, Ltd.
Product code	GEX
Device class	Class II
Decision date	Jan 22, 2002
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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DIOMED 15 DIODE LASER

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