Donna received her results on Monday bright and early, I didn’t get mine until this afternoon. So in a way I already figured what my results would be, because of our situation, whatever she was I was, sure to be as well.
SARS-COV-2 (COVID-19), DIAGNOSTIC
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Performed at: 01 – LabCorp Seattle
550 17th Avenue Ste 300
Seattle, WA 98122
Lab Director: Xxxxxx Xxxxxxx MD, Phone: XXX-XXX-XXXX
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Testing was performed using the Aptima SARS-CoV-2 assay. This nucleic acid amplification test was developed and its performance characteristics determined by LabCorp Laboratories. Nucleic acid amplification tests include PCR and TMA. This test has not been FDA cleared or approved. This test has been authorized by FDA under an Emergency Use Authorization (EUA). This test is only authorized for the duration of time the declaration that circumstances exist justifying the authorization of the emergency use of in vitro diagnostic tests for detection of SARS-CoV-2 virus and/or diagnosis of COVID-19 infection under section 564(b)(1) of the Act, 21 U.S.C. 360bbb-3(b) (1), unless the authorization is terminated or revoked sooner.
When diagnostic testing is negative, the possibility of a false negative result should be considered in the context of a patient’s recent exposures and the presence of clinical signs and symptoms consistent with COVID-19. An individual without symptoms of COVID-19 and who is not shedding SARS-CoV-2 virus would expect to have a negative (not detected) result in this assay.
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Component Results
SARS-CoV-2 (COVID-19) by RT-PCR | |
Standard Range | Not Detected |
Your Value | Not Detected |
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Collected on 10/16/2020 12:02 PM from Nasopharynx (Swab)
Resulted on 10/17/2020 10:05 PM
Result Status: Final result