K-number	K140029
Device name	AMIPLIVUE HSV 1&2 ASSAY
Applicant	Quidel Corporation
Product code	OQO
Device class	Class II
Decision date	Mar 26, 2014
Decision	Substantially Equivalent
Regulation	866.3305

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Source

View the full FDA submission: accessdata.fda.gov

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AMIPLIVUE HSV 1&2 ASSAY

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