RAD. THERAPY PLANNING SUP. SYS.

RAD. THERAPY PLANNING SUP. SYS. is an FDA 510(k)-cleared medical device (K772305) manufactured by Ohio Nuclear, 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 January 8, 1978. Regulation: 8.