OLYMPUS ENDOSCOPIC LIGATION DEVICE

OLYMPUS ENDOSCOPIC LIGATION DEVICE is an FDA 510(k)-cleared medical device (K001744) manufactured by Olympus America, 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 February 26, 2001. Regulation: 8.