#Rite aid covid test serial

It has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens, and 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 Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. It has been authorized by the FDA under an emergency use authorization. The BinaxNOW COVID-19 Antigen Self-Test has not been FDA cleared or approved. For any questions you may have regarding FSAs or HSAs, please browse our FAQ. This item is FSA and HSA eligible, contact your health insurance provider to determine reimbursement eligibility.Know your result now, without a need to wait for results from your healthcare provider.Perform simple test procedure using a minimally invasive nasal swab.Includes illustrated step-by-step instructions.*Abbott conducted a computational analysis of the detection of multiple SARS-COV-2 strains, including the Delta and Omicron variants, and predicts no impact to the performance of our BinaxNOW COVID-19 Antigen Self Test. when returning from a trip abroad.ĭetects multiple COVID-19 strains, including the Delta and Omicron variants* This test does NOT meet the CDC testing requirements to enter the U.S. For symptomatic use, a single test can be used.

#Rite aid covid test serial

For serial testing, simply test yourself twice over 3 days, with at least 24 hours (and no more than 48 hours) between tests. This 15-minute test can be completed anytime, anywhere. Authorization for self-testing without the need to ship samples to a lab or for a prescription from your healthcare provider. This test has received FDA Emergency Use.

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