K-number	K852969
Device name	ROTACLONE ROTAVIRUS DIAGNOSTIC KIT
Applicant	Cambridge Bioscience Corp.
Product code	LIQ
Device class	Class I
Decision date	Nov 5, 1985
Decision	Substantially Equivalent
Regulation	866.3405

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View the full FDA submission: accessdata.fda.gov

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ROTACLONE ROTAVIRUS DIAGNOSTIC KIT

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