The software can determine the extent and severity of coronary plaque build-up implicated in coronary artery disease.

Epredia has received 510(k) clearance from the FDA for the E1000 Dx, a scanner designed to streamline laboratory cancer ...

The detection feature – not the history feature covered by the MDDT qualification – was approved by the FDA in 2022. The 5th Medical Device Software Development Summit is your must-attend ...

Almost a third of medical device adverse events (AEs) were reported by manufacturers later than the US Food and Drug Administration’s (FDA) required 30-day window across a three-year period ...

Beginning Friday night, FDA employees overseeing medical devices and other key areas received calls and emails notifying them that their recent terminations had been “rescinded effective ...

Lungpacer Medical announced that it received FDA investigational device exemption (IDE) approval to begin a trial for its ...

Beginning Friday night, FDA employees overseeing medical devices and other key areas received calls and emails notifying them that their recent terminations had been “rescinded effective ...

Beginning Friday night, FDA employees overseeing medical devices, food ingredients and other key areas received calls and emails notifying them that their recent terminations had been “rescinded ...

FDA Moves to Rehire Medical Device, Food Safety and Other Staffers Fired Days Earlier WASHINGTON (AP) — Barely a week after mass firings at the Food and Drug Administration, some probationary ...