BIRD (VDR) SINUSOIDAL PERCUSSIONATORS

BIRD (VDR) SINUSOIDAL PERCUSSIONATORS is an FDA 510(k)-cleared medical device (K895486) 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 12, 1989. Regulation: 8.