MODIFICATION OF VENTURI VENTILATOR

MODIFICATION OF VENTURI VENTILATOR is an FDA 510(k)-cleared medical device (K990429) manufactured by Cardiopulmonary 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 February 23, 1999. Regulation: 8.