INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS

INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS is an FDA 510(k)-cleared medical device (K924600) manufactured by Cordis Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 9, 1992. Regulation: 8.