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3 Reasons Why Test-to-Treat is the Way of the Future
April 21, 2022
The next generation of test-to-treat diagnostics is here, and we’re on a mission to make healthcare accessible to all.
The next generation of test-to-treat diagnostics is here, and we’re on a mission to make healthcare accessible to all.
As of January 15, private insurance companies are required to reimburse members for at-home COVID-19 test purchases. Read and learn how to obtain your reimbursement.
Confused on the differences between COVID-19 tests? In this blog, we’re covering everything you need to know about diagnostic tests, antigen tests, and antibody tests.
This home test kit has not been FDA cleared or approved. This home test kit has been authorized by FDA under EUA. This home test kit has been authorized only for the testing of nasal swabs for detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This home test kit is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of IVDs for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or revoked sooner.
These self-tests have been authorized by Health Canada under an Interim Order Authorization. The Lucira COVID-19 & Flu Test has been authorized only for the testing of nasal swabs from symptomatic individuals for the detection of nucleic acid from SARS-CoV-2, influenza A, and influenza B, not for any other viruses or pathogens. The Lucira COVID-19 Test has been authorized for testing of nasal swabs from individuals with or without symptoms for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens.
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