''FUJIFILM Medical Systems USA is pleased to announce that Food and Drug Administration (FDA) 510(k) approval has been received for the Fuji Digital Radiography (FDR) AcSelerate system, making it available for sale in the U.S. A fully automated digital ...'

''The U.S. Food and Drug Administration says it has issued interim recommendations to address concerns about excess radiation exposure in medical facilities. The FDA said its recommendations are part of an ongoing investigation into cases of excess ...'

''The U.S. Food and Drug Administration today announced an initiative to reduce unnecessary radiation exposure from three types of medical imaging procedures: computed tomography (CT), nuclear medicine studies, and fluoroscopy. These procedures are the ...'

''Medical radiation, used to diagnose and treat patients, has saved countless lives in this country. But some doctors now warn that more needs to be done to ensure that the technology is used more safely. The U.S. Food and Drug Administration (FDA) said ...'

''Royal Philips Electronics NV (PHIA.AE) has received a U.S. Food and Drug Administration warning letter citing several issues the agency found during an inspection of a Cleveland facility where Philips makes computed tomography and nuclear medicine ...'

''The U.S. Food and Drug Administration (FDA) Sept. 30 cleared the world's first photon-counting computed tomography (CT) scanner, the Siemens Naeotom Alpha. Both the FDA and CT experts say this is the start of a revolution in new CT scanner technology, ...'

''Bracco Diagnostics Inc. announced U.S. Food and Drug Administration (FDA) approval for Varibar Thin Liquid (barium sulfate) for oral suspension, which is indicated for modified barium swallow (MBS) studies. The contrast agent is used to detect and ...'

''The U.S. Food and Drug Administration today announced that it is easing the pathway to market for mammography systems that produce computerized X-ray images of the entire breast. These systems, known as Full Field Digital Mammography Systems, are an ...'

''Lantheus Medical Imaging, Inc., a worldwide leader in diagnostic imaging, today announced that it has reached agreement with the U.S. Food and Drug Administration (FDA) regarding a Special Protocol Assessment (SPA) on the design and planned analysis of a ...'

''AREVA announced today that its subsidiary AREVA Med, which specializes in nuclear medicine, has received authorization from the Food and Drug Administration (FDA) to begin U.S. clinical trials for a new treatment aimed at combating cancer. This is the ...'