K-number	K070536
Device name	MEDILAS D FAMILY LASERS
Applicant	Dornier Medtech America, Inc.
Product code	GEX
Device class	Class II
Decision date	May 21, 2007
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MEDILAS D FAMILY LASERS

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