PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN

PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN is an FDA 510(k)-cleared medical device (K900314) manufactured by Percussionaire 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 October 25, 1990. Regulation: 8.