MAGNETOM AVANTO MR SYSTEM

MAGNETOM AVANTO MR SYSTEM is an FDA 510(k)-cleared medical device (K032428) 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 October 15, 2003. Regulation: 8.