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In accordance with FDA Policy for Diagnostic Tests for Coronavirus Disease-2019, we are not selling tests to the general public at this time. Please review our Terms and Conditions at Checkout and confirm you are an eligible purchaser. All orders are being evaluated due to stricter FDA guidelines. If we deem your order is not for professional use then a refund will be given and your order will be cancelled. The FDA has received the necessary intent to launch notices for the COVID-19 IgG/IgM Rapid Test Cassette sold on this website. For additional information regarding the FDA's Emergency Use Authorization (EUA) for In Vitro Diagnostic Products, please visit this link. This test's EUA Submission Number is EUA200056.

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