SIEMENS FIO2 SENSOR

SIEMENS FIO2 SENSOR is an FDA 510(k)-cleared medical device (K991884) 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 November 2, 1999. Regulation: 8.