CODMAN BACTISEAL BARIUM STRIPED CATHETERS

CODMAN BACTISEAL BARIUM STRIPED CATHETERS is an FDA 510(k)-cleared medical device (K031123) manufactured by Codman & Shurtleff, 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 May 13, 2003. Regulation: 8.