K-number	K943812
Device name	VIDAS LYME SCREEN II
Applicant	Biomerieux Vitek, Inc.
Product code	LSR
Device class	Class II
Decision date	Jun 13, 1995
Decision	Substantially Equivalent
Regulation	866.3830

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View the full FDA submission: accessdata.fda.gov

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VIDAS LYME SCREEN II

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