Covid-19 Testing

FDA Emergency Use Authorization Letters:

Assure COVID-19 IgG/IgM Rapid Test Device
COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma

1copy COVID-19 qPCR Multi Kit

Food and Drug Administration (FDA) issue an Emergency Use Authorization (EUA) for emergency use of your product, 2 pursuant to Section 564 of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. §360bbb-3)