K-number	K853399
Device name	VIROGEN ROTATEST SLIDE TEST
Applicant	Armkel, LLC
Product code	LIQ
Device class	Class I
Decision date	Nov 12, 1985
Decision	Substantially Equivalent
Regulation	866.3405

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View the full FDA submission: accessdata.fda.gov

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VIROGEN ROTATEST SLIDE TEST

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