KION ANESTHESIA SYSTEM

KION ANESTHESIA SYSTEM is an FDA 510(k)-cleared medical device (K973971) manufactured by Siemens Medical Solutions USA, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 12, 1999. Regulation: 8.