We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
A rapid method for detecting and identifying very small numbers of diverse bacteria, from anthrax to E. coli, has been developed by scientists from the National Cancer Institute (NCI) and National Institute of Standards and Technology (NIST).
Sicel Technologies announced that DVS (dose verification system), its wireless implantable radiation sensor and reader, has received 510(k) clearance from the FDA.
St. Jude Medical today announced FDA approval and market launch of its Merlin Patient Care System, a universal programmer for implantable cardioverter defibrillators (ICDs) and pacemakers.
The federal government is proposing a sweeping overhaul of how it pays hospitals for heart-device implants and other high-priced medical procedures, a change that could cut into sales for Boston Scientific and other companies that make medical devices.
Boca Medical Products has issued a recall of 3,984 boxes of its Ultilet Insulin Syringe 30g 1/2cc product lot, number 5GEXI, as displayed on the inner case.
The FDA will rely on a panel of outside medical experts in cardiac electrophysiology to help determine the safety and effectiveness of defibrillators already on the market, particularly in cases when a device is recalled.