SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST

SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST is an FDA 510(k)-cleared medical device (K924489) 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 January 14, 1993. Regulation: 8.