ARIX RAD ACQUISITION CONSOLE

ARIX RAD ACQUISITION CONSOLE is an FDA 510(k)-cleared medical device (K123650) manufactured by Compania Mexicana DE Radiologia Cgr, S.A. DE C.V.. 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 19, 2013. Regulation: 8.