DAVIS+GECK ABSORBABLE LIGATING DEVICE

DAVIS+GECK ABSORBABLE LIGATING DEVICE is an FDA 510(k)-cleared medical device (K925602) manufactured by Davis & Geck, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 7, 1993. Regulation: 8.