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Home » ViewRay Gets 510(k) Clearance for Its MRIdian MRI-Guided Radiation Therapy Software
ViewRay Gets 510(k) Clearance for Its MRIdian MRI-Guided Radiation Therapy Software
ViewRay has received the FDA’s 510(k) clearance for its next generation of magnetic resonance imaging (MRI)-guided radiation therapy software.
MRIdian A3i includes new features to streamline on-table adaptive workflow and reduce treatment times, the Cleveland, Ohio-based company said.
The new version of the software also includes a new brain treatment package expanding its clinical utility into cranial stereotactic radiosurgery and stereotactic radiation therapy.
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