*The BD Veritor™，™SARS-CoV-2nucleocapsid antigens in direct anterior nasal swabs from individuals who are either suspected of COVID-19by their health care provider within the first five days of the onset of symptoms， or from individuals without symptoms or other epidemiological reasons to suspect COVID-19when tested twice over two or three days with at least24hours and no more than48hours between tests。
This product has not been FDA cleared or approved；but has been authorized by FDA under an EUA foruse by authorized laboratories。
RSV=respiratory syncytial virus；SARS-CoV-2=severe acute respiratory syndrome coronavirus2。
This product has been authorized only for the detection of proteins from SARS-CoV-2，not for any other viruses or pathogens。
This product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section564（b）（1）of the Federal Food，Drug and Cosmetic Act，21U.S.C.30bb-3（b）（b）（1），1），unless the declaration is terminated，or authorization is revoked sooner。
Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988（CLIA），42U.S.C§263a，that meet the requirements to perform moderate，high or waived complexity tests.This test is authorized for use at the Point of Care（POC），i.e.，in patient care settings operating under a CLIA Certificate of Waiver，Certificate of Compliance，or Certificate of Accreditation。
