iSnare system-Lariat

iSnare system-Lariat is an FDA 510(k)-cleared medical device (K152035) manufactured by United States Endoscopy Group, 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 October 14, 2015. Regulation: 8.