MODEL 7200AE VENTILATOR FLOW BY 2.0 OR OPTION 50

MODEL 7200AE VENTILATOR FLOW BY 2.0 OR OPTION 50 is an FDA 510(k)-cleared medical device (K920002) manufactured by Puritan Bennett Corp.. 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 9, 1992. Regulation: 8.