K-number	K101712
Device name	ENDOVASCULAR LAER VEIN SYSTEM KIT
Applicant	Biolitec, Inc.
Product code	GEX
Device class	Class II
Decision date	Oct 27, 2010
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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ENDOVASCULAR LAER VEIN SYSTEM KIT

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