The US Food and Drug Administration (FDA) has granted 510(k) clearance for the first MRI device designed specifically for brain and head imaging of newborns in the neonatal intensive care unit (NICU).
On July 20, 2017, the Food and Drug Administration announced the clearance of “the first magnetic resonance imaging (MRI) device specifically for neonatal brain and head imaging in neonatal intensive ...
A new portable MRI device detected specific brain abnormalities in 29 of 30 patients taken to Yale New Haven Hospital’s neuroscience intensive care unit after presenting with symptoms of stroke and ...
A technology being developed at Purdue University could provide an affordable, smart, self-learning device that, when placed into existing MRI machines could allow medical professionals to monitor ...
A study published in the journal JAMA Neurology is reporting promising results testing the world’s first portable MRI machine in a real-world intensive care setting. The groundbreaking device ...
WEST LAFAYETTE, Ind. – A Purdue-affiliated startup, MR-Link LLC, is developing a coin-sized, affordable device that once inserted into existing MRI machines could allow researchers and medical ...
Yale researchers have agreed to develop, deploy, and test a new portable MRI scanner, a device its developer hopes will cost a fraction of that of traditional MRIs and make the new imaging technology ...
Patients who have pacemakers or defibrillators are often denied the opportunity to undergo magnetic resonance imaging (MRI) because of safety concerns, unless the devices meet certain criteria ...
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