MGB LAPALUX TELESCOPE

MGB LAPALUX TELESCOPE is an FDA 510(k)-cleared medical device (K982013) manufactured by Mgb Endoskopische Gerate GmbH. 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 20, 1998. Regulation: 8.