EXTERNAL VENTRICULAR DRAINAGE/MONITORING/LUMBAR SE

EXTERNAL VENTRICULAR DRAINAGE/MONITORING/LUMBAR SE is an FDA 510(k)-cleared medical device (K854474) 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 November 26, 1985. Regulation: 8.