LabCorp COVID-19 At-Home Test Kit Receives FDA Emergency Use Authorization
Laboratory Corporation of America Holdings (LH)
Last laboratory corporation of america holdings earnings: 4/29 06:53 am
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Source: Business Wire
Initial Distribution Prioritized for Frontline Healthcare Workers and First Responders BURLINGTON, N.C.--(BUSINESS WIRE)--LabCorp (NYSE: LH), a leading global life sciences company that is deeply integrated in guiding patient care, today announced that it has received an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA). The EUA permits nasal swab specimens to be collected at home using the Pixel by LabCorp™ COVID-19 test home collection kit if recommended by a healthcare provider after completing a COVID-19 questionnaire.LabCorp’s COVID-19 at-home test kit is part of the company’s continued commitment to increase the supply and availability of tests for healthcare workers and first responders who have symptoms consistent with COVID-19. Enabling individuals to self-administer sample collection will help prevent the risk of transmitting the virus to others and reduces the demand for personal protective equipment (PPE) as the tests do not require a cl
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LH
Earnings
- 10/28/25 - Beat
LH
Sec Filings
- 12/3/25 - Form 4
- 12/3/25 - Form 3
- 11/24/25 - Form 8-K
- LH's page on the SEC website