VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS

VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS is an FDA 510(k)-cleared medical device (K905235) 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 May 2, 1991. Regulation: 8.