Co-Diagnostics Announced That It Submitted Its Co-DX PCR COVID-19 Test With Co-Dx PCR PRO Instrument For Review By The FDA For Emergency Use Authorization
Portfolio Pulse from Benzinga Newsdesk
Co-Diagnostics has submitted its Co-DX PCR COVID-19 test and Co-Dx PCR PRO instrument for FDA Emergency Use Authorization. The platform aims to support point-of-care and at-home testing, with a development pipeline including tests for TB, HPV, and a multiplex respiratory panel for flu A/B, COVID-19, and RSV.
December 27, 2023 | 2:32 pm
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Co-Diagnostics has submitted its Co-DX PCR COVID-19 test and Co-Dx PCR PRO instrument for FDA Emergency Use Authorization, potentially expanding its product offerings and market reach.
The submission for FDA Emergency Use Authorization is a significant step for Co-Diagnostics, indicating potential growth in its product line and market presence. If approved, it could lead to increased sales and market share, positively impacting the stock price in the short term.
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