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LabCorp
The U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for LapCorp s Pixel COVID-19 Test At-Home Collection Kit, the first at-home COVID-19 test kit that doesn’t require a doctor’s prescription for purchase.
The approval, announced by the FDA on December 9, will allow people older than 18 to collect their own nasal swab at home and send it to LabCorp for analysis and results.
Positive or invalid test results are delivered to the user by a healthcare provider. If a person tests negative, the results are sent via email or an online portal. Once the test is received at the LabCorp facility, average time to deliver the results is currently one to two days, according to the company s website.