VIBRALUNG ACOUSTICAL PERCUSSOR

VIBRALUNG ACOUSTICAL PERCUSSOR is an FDA 510(k)-cleared medical device (K133057) manufactured by Westmed, 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 May 22, 2014. Regulation: 8.