K-number	K070747
Device name	QUICK VUE RSV TEST, MODELS 20193, 20199
Applicant	Quidel Corp.
Product code	GQG
Device class	Class I
Decision date	Apr 23, 2007
Decision	Substantially Equivalent
Regulation	866.3480

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View the full FDA submission: accessdata.fda.gov

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QUICK VUE RSV TEST, MODELS 20193, 20199

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