K-number	K141931
Device name	LYRA ADENOVIRUS ASSAY
Applicant	Quidel Corporation
Product code	OCC
Device class	Class II
Decision date	Oct 9, 2014
Decision	Substantially Equivalent
Regulation	866.3980

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Source

View the full FDA submission: accessdata.fda.gov

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LYRA ADENOVIRUS ASSAY

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