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.
Market News and Data brought to you by Benzinga APIs
Comments
Loading...
Posted In: NewsPenny StocksHealth CareFDAGeneralBriefsCovid-19Emergency Use Authorization
Benzinga simplifies the market for smarter investing

Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.

Join Now: Free!