The FDA cleared an extended version of Neurophet AQUA that uses AI for analysis in counting and measuring MS brain lesions on ...

New study finds that AI didn't help reduce radiologists' burnout, HHS called out for not auditing HIPAA compliance, and more.

The FDA will discuss a new framework for regulating generative artificial intelligence (GenAI)-enabled medical devices.

Augmedics has received the Food and Drug Administration (FDA) 510(k) clearance of the new CT-to-fluoroscopy (CT-Fluoro) registration method for its xvision spine system. Navigating off using ...

The Food and Drug Administration will hold its first Digital Health Advisory Committee (DHAC) meeting to discuss how the ...

The FDA's digital health advisory committee is expected to weigh in on how generative AI should be regulated by the agency.

The software is designed to improve the accuracy of detecting morphological abnormalities during foetal heart ultrasound ...

BrightHeart, a leading AI innovator in obstetric and pediatric cardiology technology, announces it has received FDA 510(k) clearance for its first artificial intelligence software, designed to ...

Good afternoon, ladies and gentlemen, and welcome to the Perimeter Medical Q3 2024 Conference Call. At this time, all lines are in listen-only mode. [Operator Instructions]. This call is being ...

Cortechs.ai is the only organization capable of processing both GRE and SWI sequences—settin a new standard for comprehensive and reliable imaging solutions. This capability is essential in today's ...