CODMAN LASER NEUROENDOSCOPE

CODMAN LASER NEUROENDOSCOPE is an FDA 510(k)-cleared medical device (K924977) 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 November 21, 1993. Regulation: 8.