La Jolla, CA - Just as some of the first so-called "MRI-safe" implantable cardiac devices are starting to seek FDA approval, leaders of the first large registry to address MRI safety are cautioning ...

Background: A relaxation of the prohibition of scanning cardiac rhythm device patients is underway, largely because of the growing experience of safe scanning events at 1.5T. Magnetic resonance ...

The Food and Drug Administration on Thursday approved Aspect Imaging’s MRI device for infants in the neonatal intensive care unit. The Embrace Neonatal MRI System, which is specially designed for ...

Please provide your email address to receive an email when new articles are posted on . An analysis of more 800 MRI examinations shows the scans do not induce clinically significant functional changes ...

Machine learning enables cheaper and safer low-power magnetic resonance imaging (MRI) without sacrificing accuracy, according to a new study. According to the authors, these advances pave the way for ...

(WASHINGTON) — The U.S. Food and Drug Administration on Thursday approved the first MRI device specifically for neonatal brain and head imaging in neonatal intensive care units. “Although we can use ...

More than 60 million magnetic resonance imaging (MRI) scans are performed worldwide each year, but imaging for the millions of patients with cardiac implantable electronic devices (CIEDs) such as ...

The Kivalliq Health Centre in Rankin Inlet now has a Hyperfine Swoop portable head magnetic resonance imaging (MRI) device ...

Philips North America is recalling 150 MRI machines in the U.S. due to explosion risks. The FDA has classified the recall as a Class 1, the most serious type of recall. Two models of the Panorama 1.0T ...