ACT 11 MP VENTRICULAR CATHETER

ACT 11 MP VENTRICULAR CATHETER is an FDA 510(k)-cleared medical device (K013005) manufactured by Innerspace, 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 March 7, 2002. Regulation: 8.