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home / news releases / HOLX - FDA OKs emergency use of Hologic high-throughput COVID-19 molecular test


HOLX - FDA OKs emergency use of Hologic high-throughput COVID-19 molecular test

Hologic (HOLX) announces emergency use authorization in the U.S. for its Panther Fusion SARS-CoV-2 molecular assay for use in testing asymptomatic people for COVID-19 infection (in other words, the high-throughput test can be used to screen people who may have been exposed to an infected person).The automated Panther Fusion system can generate initial results in ~three hours and more than 1,000 coronavirus tests in 24 hours.Shares up 3% premarket on light volume.

For further details see:

FDA OKs emergency use of Hologic high-throughput COVID-19 molecular test
Stock Information

Company Name: Hologic Inc.
Stock Symbol: HOLX
Market: NASDAQ
Website: hologic.com

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