NEWPORT WAVE VENTILATOR MODEL E200

NEWPORT WAVE VENTILATOR MODEL E200 is an FDA 510(k)-cleared medical device (K901785) manufactured by Newport Medical Instruments, 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 August 9, 1990. Regulation: 8.