FDA grants breakthrough status to Aidoc’s AI radiology report system
The US Food and Drug Administration (FDA) has granted breakthrough device designation to Aidoc’s First Read, an AI system that…
The US Food and Drug Administration (FDA) has granted breakthrough device designation to Aidoc’s First Read, an AI system that…
Johnson & Johnson (J&J) has initiated enrolment in its SKYWARD investigational device exemption (IDE) clinical programme to evaluate the Shockwave…
Oracle Health has entered a collaboration with Theator to bring AI-powered surgical intelligence solutions to its US customer base. The…
Quest Diagnostics has received approval from the New York State Department of Health's (NYSDOH) Clinical Laboratory Evaluation Programme for its…
Researchers from the University of Florida (UF) Health Cancer Institute in the US are developing a rapid, non-invasive urine test…
CereVasc has concluded patient enrolment in its STRIDE pivotal study, assessing the safety and effectiveness of the investigational eShunt System…
Speciality diagnostics solutions developer Masimo has received 510(k) clearance from the US Food and Drug Administration (FDA) for an opioid-induced…
Labcorp has announced the availability of ColoSense, its ribonucleic acid (RNA)-based at-home screening test for colorectal cancer that has been…
Neko Health has introduced new body composition and wearables integration features to its health scan service, marking what it describes…
Imperative Care has reported results from a post-hoc analysis of the SYMPHONY-PE trial, assessing the role of early mechanical thrombectomy…