DAVIS & GECK LIGATING CLIP REMOVER

DAVIS & GECK LIGATING CLIP REMOVER is an FDA 510(k)-cleared medical device (K953908) manufactured by Davis & Geck, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 29, 1995. Regulation: 8.