MEDISONIC PNEU-NEB

MEDISONIC PNEU-NEB is an FDA 510(k)-cleared medical device (K896192) manufactured by Medisonic U.S.A., 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 January 2, 1990. Regulation: 8.