''Bayer announced that Ultravist (iopromide)-300, -370, its iodine-based contrast agent, has been approved by the U.S. Food and Drug Administration (FDA) for contrast-enhanced mammography(CEM) – making it the only contrast agent approved for this ...'

''Keya Medical has launched the DeepVessel FFR, a software device that utilizes deep learning to facilitate fractional flow reserve (FFR) assessment based on coronary computed tomography angiography (CCTA). Cleared by the Food and Drug Administration ...'

''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, ...'

''Hologic, Inc., an innovative medical technology company primarily focused on improving women's health, announced U.S. Food and Drug Administration (FDA) clearance and commercial availability of the Company's Genius AI Detection technology, a new deep ...'

''The practice of CT intravenous contrast media (CM) administration has been continuously debated and updated1; however, performance of power injection systems has largely gone unstudied. Previous publications have focused on workflow efficiency as the ...'

''DUBAI GE Healthcare unveiled more than two dozen new products at the Arab Health 2020 annual meeting Monday three of which are awaiting approval in the United States. After securing 510(k) approval from the U.S. Food & Drug Administration, these ...'

''RadioMedix Inc. and its commercial partner Curium announced today that the New Drug Application for copper Cu 64 dotatate injection was filed with the U.S. Food and Drug Administration (FDA). Copper Cu 64 dotatate injection is a PET diagnostic agent ...'

''Canon Medical Systems USA Inc. has received U.S. Food and Drug Administration (FDA) 510(k) clearance on its Advanced Intelligent Clear-IQ Engine (AiCE) for the Aquilion Precision computed tomography (CT) system. The clearance further expands access to ...'

''maging centers will get a little bit of relief under a final rule issued by the Trump administration in a bid to ease regulatory burdens on healthcare providers. CMS recently issued the sweeping new legislation as part of its Patients Over Paperwork ...'

''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 ...'