Syngo Dynamics (Version VA40F)

Syngo Dynamics (Version VA40F) is an FDA 510(k)-cleared medical device (K222428) 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 November 13, 2022. Regulation: 8.