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FDA approves at-home sample collection kit for coronavirus

WASHINGTON, D.C. – The Food and Drug Administration announced Saturday that it has authorized an at-home sample collection kit that can then be sent to specified laboratories for COVID-19 diagnostic ...
RAPS

FDA issues EUA for saliva-based COVID-19 test, provides path for wider home sample collection

The US Food and Drug Administration (FDA) on Friday granted the first emergency use authorization (EUA) allowing for at-home saliva sample collection for a coronavirus disease (COVID-19) diagnostic ...
RAPS

FDA authorizes first COVID-19 test for at-home sample collection

The US Food and Drug Administration (FDA) on Tuesday granted an emergency use authorization (EUA) to LabCorp allowing it to test self-collected nasal swab samples from patients for coronavirus disease ...
Business Wire

Rheonix COVID-19™ MDx Assay Receives Expanded FDA Emergency Use Authorization to Include ...

ITHACA, N.Y.--(BUSINESS WIRE)--Rheonix Inc. announced today that the United States Food and Drug Administration (FDA) has issued an expanded Emergency Use Authorization (EUA) for the Rheonix COVID-19™ ...
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Labcorp Gets FDA EUA For Pixel COVID-19+Flu+RSV Test Home Collection Kit

(RTTNews) - Life sciences company Labcorp (LH) announced Wednesday the receipt of Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) for a combined at-home collection ...
Business Wire

MagBio Receives 510(k) Clearance and CE Mark for MagXtract Collection Tube For COVID-19 Testing

Now Launching in U.S. and Europe as the first FDA-cleared Guanidine-Free Molecular Transport Medium; Offers Improved Safety, Stability and Cost-Effectiveness GAITHERSBURG, Md.--(BUSINESS WIRE)--MagBio ...