MODEL 2500 PNEUMATIC PERCUSSOR

MODEL 2500 PNEUMATIC PERCUSSOR is an FDA 510(k)-cleared medical device (K802399) manufactured by Medical Equipment Development Co., 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 October 22, 1980. Regulation: 8.