THE MCSHIRLEY PERCUSSOR

THE MCSHIRLEY PERCUSSOR is an FDA 510(k)-cleared medical device (K801982) manufactured by Mcshirley Products, 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 September 15, 1980. Regulation: 8.