FDA Expands EUA For Rapid Extraction On One COVID-19 Test System

  • Enzo Biochem Inc ENZ has received an expansion of its FDA Emergency Use Authorization (EUA) for its rapid extraction method on its Ampiprobe SARS-CoV-2 Test System to detect SARS-CoV-2, including the variants.
  • The EUA enables laboratories to immediately use Enzo's faster extraction process to reduce the time by over one hour, or more than 25%, allowing more test runs on a single instrument. 
  • Price Action: ENZ shares are up 11.70 at $3.43 during the premarket session on the last check Tuesday.
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