The U.S. Food and Drug Administration (FDA) announced the authorization of the test on Dec. 28.
The test was designed by Siemens Healthineers and can now be used in addition to the Roche test the FDA recently approved. The authorization comes as test shortages have wracked the nation amid record-breaking numbers of COVID-19 infections. Officials with the Biden administration praised the FDA’s move as in keeping with its COVID priorities.
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