Medical Device Network on MSN1d
FDA tags Becton, Dickinson and Company infusion software recall as Class IProblematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
The FDA has extended its review of the ProSense cryoablation system for early-stage breast cancer, with a decision expected ...
The state is using roadside tests to check whether drivers have used drugs, similar to tests for alcohol. A pilot program found that 87 percent of tested drivers had used cannabis or illegal drugs.
The Food and Drug Administration has identified a Class I recall of Medtronic Neurovascular 027 Compatible Pipeline Vantage ...
The U.S. Food and Drug Administration issued a Class II recall notice to take back 8,242 cases (197,808 cans) of Good & ...
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
With Keytruda, the best-selling drug in the world, facing the end of exclusivity in 2028, BioSpace looks at five drugs that ...
Medical Device Network on MSN3d
FDA tags Medtronic embolisation device recall as Class IMedtronic initiated the recall of certain Pipeline Vantage embolisation devices in January 2025 following reports of four ...
XBeta founder Frederick Kruger offers advice for medical device startups based on his firm's development of the Spiro Wave ...
Sooma announced that it received FDA investigational device exemption (IDE) for its transcranial direct current stimulation ...
THE Food and Drug Administration (FDA) has launched an online application process for Certificate of Medical Device ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback