PNEU PAC VENTILATOR/RESUSCITATORS

PNEU PAC VENTILATOR/RESUSCITATORS is an FDA 510(k)-cleared medical device (K832700) manufactured by Pneupac , Ltd.. 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 13, 1983. Regulation: 8.