technologynetworks

Thermo Fisher Scientific Announces 510(k) Clearance of Molecular Clinical Test for SARS-CoV-2, Flu A, Flu B and RSV

Thermo Fisher Scientific has received 510(k) clearance from the U.S. Food & Drug Administration (FDA) for the Applied Biosystems™ TaqPath™ COVID-19, Flu A, Flu B, RSV Select Panel, offering a single ...
The New England Journal of Medicine

Persistent False Positive Covid-19 Rapid Antigen Tests

Rapid antigen tests for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are effective tools for the diagnosis of acute infection, particularly when used serially. 1 The percentage of ...
Yahoo Finance

Nuclein Receives Dual FDA 510(k) Clearance and CLIA Waiver for DASH® SARS-CoV-2 & Flu A/B Test for use on the DASH® Rapid PCR System

AUSTIN, Texas, Jan. 6, 2025 /PRNewswire/ -- Nuclein, a leader in rapid, point-of-care molecular diagnostics, today announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance ...
Healio

SARS-CoV-2 protein detectable in COVID-19 patients up to 14 months after illness

Please provide your email address to receive an email when new articles are posted on . Of plasma samples taken after COVID-19 infection, 7.5% to 12.6% contained detectable viral antigens. Researchers ...