I.P.P.B. MANIFOLDS & NEB. SING. & DBL

I.P.P.B. MANIFOLDS & NEB. SING. & DBL is an FDA 510(k)-cleared medical device (K791820) manufactured by Airlife, 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 September 25, 1979. Regulation: 8.