FDA Clears Prodesse’s ProFASTâ¢+ Assay To Identify Three Strains Of Influenza A, Including 2009 H1N1
Gen-Probe Incorporated (Nasdaq: GPRO) announced that the U.S. Food and Drug Administration (FDA) has cleared for marketing Prodesse's ProFASTâ¢+ assay, making it the only FDA-cleared molecular diagnostic test to simultaneously detect and differentiate three common influenza A virus subtypes seasonal A/H1, seasonal A/H3, and 2009 H1N1. "FDA clearance of our ProFAST+ assay is important for public health, as the test enables physicians to accurately differentiate among influenza A subtypes that have different antiviral susceptibilities," said Carl Hull, Gen-Probe's president and CEO... (Source: Health News from Medical News Today)




