FDA authorizes test to identify recent or prior COVID-19 infection
The Food and Drug Administration last week authorized for emergency use a test kit to help identify individuals with an adaptive immune response to SARS-CoV-2, indicating a recent or prior infection. Only laboratories certified under the Clinical Laboratory Improvement Amendments that meet requirements to perform high or moderate complexity tests may use the . Negative results do not preclude acute COVID-19 infection, the agency said.
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