MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI

MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI is an FDA 510(k)-cleared medical device (K932375) manufactured by Siemens Medical Solutions USA, 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 September 6, 1993. Regulation: 8.