CODMAN GAAB NEUROENDOSCOPE

CODMAN GAAB NEUROENDOSCOPE is an FDA 510(k)-cleared medical device (K923555) manufactured by Codman & Shurtleff, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 22, 1993. Regulation: 8.