MM-22 MICROTRON, MM50 MICROTRON

MM-22 MICROTRON, MM50 MICROTRON is an FDA 510(k)-cleared medical device (K900434) manufactured by Scanditronix, 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 22, 1990. Regulation: 8.