Prognostic Test for Preeclampsia Receives FDA 510(k) Clearance
Roche’s Elecsys sFlt-1/PlGF test received FDA clearance, providing a prognostic way to help ID pregnant women at risk of severe preeclampsia.
Read MorePosted by Chris Wolski | Feb 18, 2025 | Womens Health |
Roche’s Elecsys sFlt-1/PlGF test received FDA clearance, providing a prognostic way to help ID pregnant women at risk of severe preeclampsia.
Read MorePosted by Chris Wolski | Feb 18, 2025 | Covid 19 |
Hologic, Inc. has received FDA 510(k) clearance for its Aptima SARS-CoV-2 assay, initially authorized for emergency use in 2020.
Read MorePosted by Chris Wolski | Feb 13, 2025 | Molecular Diagnostics |
Thermo Fisher Scientific has received FDA 510(k) clearance for its Applied Biosystems TaqPath COVID-19, Flu A, Flu B, RSV Select Panel, a real-time PCR multiplex test.
Read MorePosted by Chris Wolski | Feb 7, 2025 | Gastrointestinal Infections |
Nearly 50 million Americans, particularly in rural areas, face barriers to seeing a gastroenterologist, needing to travel at least 25 miles.
Read MorePosted by Chris Wolski | Feb 7, 2025 | Miscellaneous |
HealthTrackRx’s new anthem video underscores its mission to combat antibiotic resistance by delivering next-morning results.
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