CPAP/PRO CPAP INTERFACE

CPAP/PRO CPAP INTERFACE is an FDA 510(k)-cleared medical device (K992384) manufactured by Stevenson Industries, 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 November 30, 1999. Regulation: 8.