OSOM® COVID-19 Antigen Rapid Test | EUA

• Trust your results – High positive percent agreement & negative percent agreement to help you reduce the risk of misdiagnosis & inappropriate treatment
• Easy-to-use – Can be performed in a CLIA-waived setting & comes with everything you need to run a test, without the need for specialized equipment
• Save valuable time – Get results to your patient in only 15 minutes
• Simple sample collection – Direct Mid-Turbinate nasal swab to help you improve patient comfort
• Get it when you need it – Proudly made in the USA & backed by a trustworthy supply chain so you can avoid delays from international shipments
• Exceptional support – Experienced support teams & online training modules to help streamline your testing implementation & staff training

This test has not been FDA cleared or approved. It is authorized by FDA under an EUA for use by authorized laboratories. It has been authorized only for the detection of SARS-CoV-2 antigen, 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 S360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.

Mid-Turbinate Swab

Product Training