MJ NEONATAL PERCUSSOR

MJ NEONATAL PERCUSSOR is an FDA 510(k)-cleared medical device (K812151) manufactured by Cussionair Therapy 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 August 24, 1981. Regulation: 8.