MALVERN, Pa.--(BUSINESS WIRE)--The Food and Drug Administration (FDA) has cleared the MAGNETOM Vida 3 Tesla (3T) magnetic resonance imaging (MRI) scanner from Siemens Healthineers, which features new ...
New pacing systems have recently been specifically designed by the major companies for safe use in the MRI environment (EnRhythm, Advisa, and Revo MRI SureScan pacemakers and CapSureFix MRI leads, ...
GE HealthCare (Nasdaq: GEHC) announced that it submitted its next-generation Signa Bolt MRI technology to the FDA for 510(k) ...
GUILFORD, Conn.--(BUSINESS WIRE)--Hyperfine Research, Inc. announced today that it has received US Food & Drug Administration 510(k) clearance for the world’s first bedside Magnetic Resonance Imaging ...
MRI is a powerful diagnostic tool, but the size and cost of the machinery limits where it can be used. Scientists at the University of Hong Kong (HKU) have now developed a more compact and affordable ...
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 ...
MINNEAPOLIS, Minnesota -- Medtronic, Inc. today announced U.S. Food and Drug Administration (FDA) approval for its Investigational Device Exemption (IDE) application and pivotal clinical trial ...
It doesn't happen often, but every now and then in this world of medical device innovation we come across a truly outside-the-box technology that has the potential to really disrupt the standard of ...
The RNS System consists of a small neurostimulator that is surgically implanted into the skull, delivering an electrical stimulation to the brain via leads when abnormal activity is detected. The Food ...
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