Symbia Pro.specta VA20A Family

Symbia Pro.specta VA20A Family is an FDA 510(k)-cleared medical device (K231102) 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 16, 2023. Regulation: 8.