CODMAN-MEDOS VALVE SHUNT SYSTEM

CODMAN-MEDOS VALVE SHUNT SYSTEM is an FDA 510(k)-cleared medical device (K944222) manufactured by Johnson & Johnson Professionals, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 27, 1995. Regulation: 8.