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Re: Farmer_D post# 3389

Sunday, 03/07/2021 12:41:57 PM

Sunday, March 07, 2021 12:41:57 PM

Post# of 4060

Abbott (NYSE: ABT) today announced U.S. Food and Drug Administration (FDA) Emergency Use Authorization (EUA) for the company's Alinity m Resp-4-Plex molecular assay to detect and differentiate SARS-CoV-2, influenza A, influenza B and respiratory syncytial virus (RSV) in one test. This is an important tool because these viruses have similar symptoms but require different treatment approaches.

I wonder when they submitted this for FDA approval and how that compares to when CODX submitted. I am trying to guess when we can expect approval.

Opti

Hebrews 11:6 And without faith it is impossible to please Him, for he who comes to God must believe that He is and that He is a rewarder of those who seek Him.

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