syngo Ultrasound Apps Suite (sUSAS)

syngo Ultrasound Apps Suite (sUSAS) is an FDA 510(k)-cleared medical device (K201062) 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 May 17, 2020. Regulation: 8.