K-number	K965092
Device name	VIDAS ROTAVIRUS ASSAY
Applicant	Biomerieux Vitek, Inc.
Product code	LIQ
Device class	Class I
Decision date	May 5, 1997
Decision	Substantially Equivalent
Regulation	866.3405

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View the full FDA submission: accessdata.fda.gov

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VIDAS ROTAVIRUS ASSAY

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