Diasorin Simplexa COVID Direct Kit Receives FDA 510(k) Clearance
DiaSorin has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Simplexa COVID-19 Direct kit.
Read MorePosted by Chris Wolski | Sep 14, 2022 | Covid 19 |
DiaSorin has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Simplexa COVID-19 Direct kit.
Read MorePosted by Chris Wolski | Sep 14, 2022 | Infectious Diseases |
Todos Medical intends to validate multiple PCR polio assays, including wastewater testing with ultra-high sensitivity.
Read MorePosted by Chris Wolski | Sep 13, 2022 | Covid 19 |
Shield T3 is now providing vending machines stocked with more than 300 of its saliva-based, PCR tests for COVID-19.
Read MorePosted by Andy Lundin | Sep 12, 2022 | Covid 19, Needles, Tubes, and Tourniquets |
MagBio Genomics, announced U.S. FDA 510(k) clearance, CE Mark approval, and global launch of its MagXtract Collection Tube.
Read MorePosted by Andy Lundin | Sep 9, 2022 | Allergy & Autoimmune, Immunoassay |
Exosome Diagnostics presented data on their novel non-invasive saliva profiling assay for Sjögren’s Syndrome diagnosis and monitoring.
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