Lariat, Hot/Cold Snare

Lariat, Hot/Cold Snare is an FDA 510(k)-cleared medical device (K200745) 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 April 20, 2020. Regulation: 8.