SERVO VENTILATOR 900 C/D

SERVO VENTILATOR 900 C/D is an FDA 510(k)-cleared medical device (K871354) manufactured by Siemens Elema AB. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 20, 1987. Regulation: 8.