PENLON ANESTHESIA VENTILATOR SERIES 300

PENLON ANESTHESIA VENTILATOR SERIES 300 is an FDA 510(k)-cleared medical device (K842363) manufactured by Bear Medical 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 June 25, 1984. Regulation: 8.