WINTER SPRINGS, Fla., Oct. 26, 2017 (GLOBE NEWSWIRE) -- IRADIMED CORPORATION (NASDAQ:IRMD), today announced FDA 510(k) clearance of its 3880 Magnetic Resonance Imaging (“MRI”) compatible patient vital ...
The US Food and Drug Administration (FDA) has approved a new software upgrade for Abbott's Infinity deep-brain stimulation (DBS) system used in patients with Parkinson's disease and essential tremor, ...
ST. PAUL, Minn., St. Jude Medical, Inc., a global medical device company, today announced that it has received European CE Mark approval for its Accent MRI(TM) pacemaker and Tendril MRI(TM) lead. The ...
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