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HOLX - FDA expands authorization of Hologic Aptima COVID-19 test
Hologic Inc.
The FDA has broadened its emergency use authorization ((EUA)) of Hologic's (HOLX) Aptima SARS-CoV-2 assay to include testing of people without symptoms or other reasons to suspect COVID-19 infection.Last week, the agency OK'd similar claims for the company's Panther Fusion SARS-CoV-2 test.