ENDOSCOPIC RETRIEVAL DEVICE

ENDOSCOPIC RETRIEVAL DEVICE is an FDA 510(k)-cleared medical device (K120084) 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 May 29, 2012. Regulation: 8.