CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS

CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K923646) 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 December 20, 1992. Regulation: 8.