BioCentury
ARTICLE | Clinical News

ProFast+ assay regulatory update

August 2, 2010 7:00 AM UTC

FDA granted 510(k) clearance for the ProFast+ assay from Gen-Probe's Prodesse Inc. subsidiary to detect and differentiate seasonal influenza A subtypes H1 and H3 and 2009 H1N1 viruses. The RT-PCR tes...