MJ PERCUSSOR(TM)

MJ PERCUSSOR(TM) is an FDA 510(k)-cleared medical device (K901026) manufactured by Merced Medical, 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 March 14, 1990. Regulation: 8.