K-number	K912666
Device name	DAKO ELISA ROTAVIRUS KIT- 96 TESTS K440
Applicant	Dako Corp.
Product code	LIQ
Device class	Class I
Decision date	Feb 14, 1992
Decision	Substantially Equivalent
Regulation	866.3405

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View the full FDA submission: accessdata.fda.gov

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DAKO ELISA ROTAVIRUS KIT- 96 TESTS K440

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