Name of Test: Annual Checkup 5 Panel - $99.99ĭescription: The Annual Checkup 5 panel test includes the following wellness tests: False positive results infrequently occurĭue to prior infection with other human Coronaviruses. Results from antibody testing should not be usedĪs the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status.
Molecular diagnostic should be considered to rule out infection in these individuals. Results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Test has been authorized only for detecting the presence of antibodies against SARS-CoV-2, not for any other viruses or pathogens. 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. Of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. This test is only authorized for the duration of theĭeclaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis This test has been authorized by FDA under an Emergency Use Authorization (EUA). This test is recommended for individualsĪt greater than or equal to 14 days post-symptom onset or following exposure to individuals with confirmed COVID-19.The incubation period Results should not be used as the sole basis to diagnosis or exclude recent SARS-CoV-2 infection. (i.e., IgG, IgA, IgM), it preferentially detects IgG antibodies since these are more likely to evolve to become high affinity.
While this assay in principle can detect high affinity antibodies of all isotypes Which are more likely to be specific for SARS-CoV-2.
This assay enriches detection of higher affinity antibodies Qualitative detection of high affinity antibodies to SARS-CoV-2, the virus that causes COVID-19, to aid in identifying individuals withĪn adaptive immune response to SARS-CoV-2, indicating recent or prior infection. The COVID-19 Antibody test is analyzed by one of our Nationally FDA/CLIA Accredited laboratories (Quest, LabCorp, Clinical Refence Labs)Īnd is authorized to conduct COVID-19 testing in accordance with
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Tube, instructions and test registration number, pre-paid overnight shipping label and biohazard containment bag. Physician will contact the donor to discuss the results and safety protocols. In as little as 24-48 hours, in the event the test is positive, immediate quarantine is recommended and a licensed Self-collection saliva test which the donor sends to the laboratory for analysis. This test is utilized for the purpose of determining if the COVID-19 Virus is active in a person’s body and is a
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