I.P.P.B., DIS. W/MANIFOLD/NEBULIZER

I.P.P.B., DIS. W/MANIFOLD/NEBULIZER is an FDA 510(k)-cleared medical device (K760221) manufactured by Manner Medical Products. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 2, 1976. Regulation: 8.