May 21, 2014 — Siemens Healthcare announced that the U.S. Food and Drug Administration (FDA) cleared the Somatom Force computed tomography (CT) system — the next generation in dual source CT. 


Patients with hypertension after renal artery stenting who do not respond to drug treatment may have another option. 


May 21, 2014 — iRhythm Technologies Inc. announced that data from four studies presented at Heart Rhythm 2014, the Heart Rhythm Society's 35th Annual Scientific Sessions, support the use of the company's Zio Service to identify atrial fibrillation (AF) and other cardiac arrhythmias.


The FDA has recognized 3-D printing technology now exists to print medical devices and is gathering information regarding technical assessments that should be considered when it will inevitably begin reviewing these types of future FDA submissions.


Sony Electronics’ Medical Systems Division showcased a full line of medical grade monitors for radiology applications, including the LMD-DM50, LMD-DM30C and LMD-DM30 models, at the 2014 Society for Imaging Informatics in Medicine (SIIM) meeting, in Long Beach, Calif.


St. Jude Medical Inc. announced that the first patient implants occurred in the Portico Re-sheathable Transcatheter Aortic Valve System U.S. IDE Trial (PORTICO trial).


May 20, 2014 — Siemens Healthcare announced the U.S. Food and Drug Administration (FDA) has cleared the 16- and 32-slice iterations of its Somatom Perspective computed tomography (CT) system.


May 20, 2014 — GE Healthcare and Tesla Engineering Ltd. are collaborating to produce 7T human whole-body magnetic resonance imaging (MRI) scanners. The companies made the announcement at the joint meeting of the International Society for Magnetic Resonance in Medicine (ISMRM) and the European Society for Magnetic Resonance in Medicine and Biology (ESMRMB) in Milan.


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