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FDA Clears OTC COVID Home Antigen Test

Posted by Andy Lundin | Nov 10, 2023 | Covid 19 |

The U.S. Food & Drug Administration (FDA) has granted 510(k) marketing clearance for this COVID-19 Antigen Home Test

Researchers demonstrated that metal-enhanced fluorescence probes could rapidly detect influenza virus proteins without complex lab equipment.

The prototype device uses lab-on-a-chip technology and has been proven to provide rapid and low-cost detection of COVID from nasal swabs.

Abbott received FDA approval for its molecular HPV screening solution for its Alinity m family of diagnostic assays.

Posted by Andy Lundin | Oct 26, 2023 | Covid 19 |

Researchers developed a novel platform that couples nanopore technology with artificial intelligence for rapid and accurate COVID testing.