CTM (CLINAC TREATMENT MONITOR)

CTM (CLINAC TREATMENT MONITOR) is an FDA 510(k)-cleared medical device (K770202) manufactured by Varian Assoc., 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 February 6, 1977. Regulation: 8.