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MRI: Page 106
FDA approves Bracco's ProHance for use in kids
By
AuntMinnie.com staff writers
The U.S. Food and Drug Administration (FDA) has approved the use of the ProHance MRI contrast agent by Bracco Diagnostics for use in MRI scans of pediatric patients.
December 22, 2020
Hyperfine lands first Fla. portable MRI installation
By
AuntMinnie.com staff writers
Hyperfine Research has announced an installation of its Swoop portable MRI scanner at the Tampa General Hospital, a comprehensive stroke center in Florida, for use in assessing critically ill patients with imaging at the point of care.
December 22, 2020
FDA clears Canon's Speeder protocol for 3D MRI
By
AuntMinnie.com staff writers
Canon Medical Systems has announced that the U.S. Food and Drug Administration (FDA) has cleared its Compressed Speeder technology for use with 3D sequences on Canon's Vantage Orian 1.5-tesla MRI system.
December 21, 2020
fMRI reveals info about visual conditions in stroke patients
By
AuntMinnie.com staff writers
Functional MRI (fMRI) reveals that a brain region in the superior temporal sulcus is crucial for processing and making decisions about visual information and could provide information to treat visual conditions arising from stroke, according to a December 17 study in
Neuron
.
December 17, 2020
Philips, InSightec to partner on MRgUS
By
AuntMinnie.com staff writers
Philips Healthcare parent Royal Philips and InSightec announced they will collaborate on an effort to make MR-guided focused ultrasound (MRgUS) for neurosurgery and neurological disorder treatment more accessible.
December 16, 2020
Manganese-based MRI agent shows promise
By
AuntMinnie.com staff writers
An MRI contrast agent based on manganese shows promise as an alternative to gadolinium-based contrast agents, according to research published in
Investigative Radiology
.
December 16, 2020
Perspectum nabs FDA funding for liver imaging biomarker
By
AuntMinnie.com staff writers
Image analysis software developer Perspectum has received funding from the U.S. Food and Drug Administration (FDA) Center for Drug Evaluation and Research to speed up the qualification of its cT1 imaging biomarker as a liver disease drug development tool.
December 15, 2020
FDA grants breakthrough device status to CardioFlux
By
AuntMinnie.com staff writers
The U.S. Food and Drug Administration (FDA) granted breakthrough device designation to biomagnetic cardiac imaging technology developer Genetesis for its CardioFlux system, which diagnoses myocardial ischemia and infarction in patients with symptoms suggestive of acute coronary syndrome.
December 14, 2020
FDA clears GE's Clariscan 5-mL glass vials
By
AuntMinnie.com staff writers
The U.S. Food and Drug Administration (FDA) has cleared GE Healthcare's 5-mL glass vial packaging for Clariscan, the company's macrocyclic gadolinium-based MRI contrast agent.
December 9, 2020
Patient report to FDA describes MRI face mask burn
By
Kate Madden Yee
A patient report submitted in October to the U.S. Food and Drug Administration (FDA) describes a third-degree burn a patient sustained while wearing a face mask during an MRI exam.
December 8, 2020
MRI radiomics predicts axillary lymph node metastasis
By
Erik L. Ridley
In patients with early-stage breast cancer, "signatures" derived from MRI radiomics and patient clinical risk characteristics can be utilized to preoperatively predict axillary lymph node metastasis as well as disease-free survival, according to research published online December 8 in
JAMA Network Open
.
December 7, 2020
FDA issues face mask warning for MRI exams
By
Kate Madden Yee
After a patient's face was burned from metal in a mask during a 3-tesla MRI scan, the U.S. Food and Drug Administration (FDA) on December 7 issued reminder guidance to patients and healthcare providers regarding wearing metal during MRI exams.
December 6, 2020
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