FDA 510(k) Applications for Medical Device Product Code "GQS"
(Antigens, Cf (Including Cf Control), Parainfluenza Virus 1-4)

FDA 510(k) Number Applicant Device Name Decision Date
K093415 DIAGNOSTIC HYBRIDS, INC. D3 FASTPOINT L-DFA PARAINFLUENZA VIRUS/ADENOVIRUS IDENTIFICATION KIT 12/23/2009


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