K-number	K110243
Device name	MEDART DIODE LASER SYSTEM & ACCESSORIES
Applicant	Medart A/S
Product code	GEX
Device class	Class II
Decision date	Jun 28, 2011
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MEDART DIODE LASER SYSTEM & ACCESSORIES

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