ProBeam 360° Proton Therapy System v2.0 (Multiroom)

ProBeam 360° Proton Therapy System v2.0 (Multiroom) is an FDA 510(k)-cleared medical device (K231863) manufactured by Varian Medical Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 5, 2023. Regulation: 8.