SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION

SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION is an FDA 510(k)-cleared medical device (K850563) manufactured by Nautilus Environmedical Systems, 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 March 11, 1985. Regulation: 8.