SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM

SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM is an FDA 510(k)-cleared medical device (K893640) 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 August 1, 1989. Regulation: 8.