FDA 510(k) Applications for Medical Device Product Code "GQP"
(Antisera, Neutralization, Parainfluenza Virus 1-4)

FDA 510(k) Number Applicant Device Name Decision Date
K981226 DAKO DIAGNOSTICS LTD. IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3 09/28/1998


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