FDA Authorize At-Home SARS-CoV-2 Rapid Antigen Lateral-Flow Test Posted: Mar 01, 2021 FDA Authorizes Point-of-Care Rapid Antigen Test for COVID-19 & Influenza A/B Posted: Oct 16, 2020 Quidel Receives Amended FDA-EUA for Rapid Antigen COVID-19 Diagnostic Assay  Posted: Jun 18, 2020 Fully-Automated VITROS® Systems Run 150 COVID-19 Blood Tests per Hour Posted: Apr 14, 2020 FDA Cleared Detection of Borrelia burgdorferi from Finger-Stick Whole Blood Specimens Posted: Sep 18, 2018 Qualitative Detection and Differentiation of Bordetella pertussis and B. parapertussis Posted: Jul 24, 2018 FDA Clearance for QuickVue® Influenza A+B Test Posted: Feb 20, 2018 FDA Clearance for Solana® C. difficile Molecular Assay Posted: May 30, 2017 FDA Clearance for Solana® Strep Complete Assay Posted: Nov 01, 2016 FDA Clearance for Quidel's Solana® Influenza A+B Assay Posted: Oct 04, 2016 A Hand-Held Molecular Diagnostic Test for Trichomoniasis - FDA Cleared Posted: Apr 07, 2015 FDA Clearance and CLIA Waiver for Strep A FIA Posted: Jan 05, 2015 Hand-Held Molecular Diagnostic Test for Group A Strep Posted: Sep 01, 2014 Real-time PCR Assay for HSV 1+2 and VZV gets FDA Clearance Posted: May 15, 2014 AmpliVue® Hand-Held Molecular Diagnostic Test for HSV Types 1 and 2 Posted: Apr 01, 2014 FDA Clearance for Quidel RSV and hMPV Molecular Tests Posted: Mar 26, 2013 FDA Clearance for Quidel AmpliVue® Hand-Held C.difficile Assay Posted: Dec 18, 2012 Quidel Gets CE Mark for Sofia® Legionella Fluorescent Immunoassay Posted: Nov 13, 2012 CE Mark for Quidel Direct Specimen Rapid PCR Test for Toxigenic C. difficile Posted: Aug 06, 2012