MAGNETOM Amira; MAGNETOM Sempra

MAGNETOM Amira; MAGNETOM Sempra is an FDA 510(k)-cleared medical device (K223343) 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 March 27, 2023. Regulation: 8.