The US Food and Drug Administration approved Abbott Laboratories’ ‘ID NOW’ COVID-19 rapid test tool
The “ID NOW” COVID-19 Rapid Test Tool from Abbott Laboratories was approved by the United States Food and Drug Administration.
This, as Abbott Laboratories claimed that its rapid test tool can generate results for as fast as five (5) minutes and also claimed that the “ID NOW” COVID-19 rapid test tool was the leading platform in the US.
According to the company, the rapid test tool was “only available in the United States” under the Emergency Use Authorization (EUA) of the United States Food and Drug Administration, adding that this would allow healthcare workers to make infection-control decisions and more structured treatment as well.
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