K-number	K112299
Device name	ENDOVASCULAR LASER VEIN SYSTEM KIT
Applicant	Biolitec Medical Devices, Inc.
Product code	GEX
Device class	Class II
Decision date	Nov 3, 2011
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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ENDOVASCULAR LASER VEIN SYSTEM KIT

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