The FDA is holding a forum this month to address MRI safety concerns and find ways to cut incidents. Industry leaders agree there should be safety standards in place, but are mixed on whether federal regulation is needed. What do you think?
The FDA is holding a forum this month to address MRI safety concerns and find ways to cut incidents. Industry leaders agree there should be safety standards in place, but are mixed on whether federal regulation is needed.
What do you think? Vote here and tell us more in the comments below.
FDA Grants Expanded 510(k) Clearance for Xenoview 3T MRI Chest Coil in GE HealthCare MRI Platforms
November 21st 2024Utilized in conjunction with hyperpolarized Xenon-129 for the assessment of lung ventilation, the chest coil can now be employed in the Signa Premier and Discovery MR750 3T MRI systems.
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