K-number	K131619
Device name	QUICKVUE INFLUENZA A+B
Applicant	Quidel Corp.
Product code	GNX
Device class	Class I
Decision date	Jun 28, 2013
Decision	Substantially Equivalent
Regulation	866.3330

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Source

View the full FDA submission: accessdata.fda.gov

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QUICKVUE INFLUENZA A+B

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