FDA 510(k) Application Details - K130398

Device Classification Name	Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus   More FDA Info for this Device
510(K) Number	K130398
Device Name	Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus
Applicant	QUIDEL CORP. 10165 MCKELLAR CT. SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	JOHN D TAMERIUS, PH.D. Other 510(k) Applications for this Contact
Regulation Number	866.3480   More FDA Info for this Regulation Number
Classification Product Code	GQG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/19/2013
Decision Date	08/13/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review