MODEL 7200A, PRESSURE VENTILATION OPTION

MODEL 7200A, PRESSURE VENTILATION OPTION is an FDA 510(k)-cleared medical device (K873151) 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 May 30, 1988. Regulation: 8.