K-number	K061008
Device name	QUICKVUE RSV (20 TEST KIT), MODEL 20193; (2 TEST KIT), MODEL 20199
Applicant	Quidel Corp.
Product code	MCE
Device class	Class I
Decision date	Sep 8, 2006
Decision	Substantially Equivalent
Regulation	866.3480

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View the full FDA submission: accessdata.fda.gov

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QUICKVUE RSV (20 TEST KIT), MODEL 20193; (2 TEST KIT), MODEL 20199

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