THE TULIP COMPANY BRANSON ANTERIOR ELEVATOR

THE TULIP COMPANY BRANSON ANTERIOR ELEVATOR is an FDA 510(k)-cleared medical device (K952936) manufactured by The Tulip Mfg. Co.. 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 29, 1995. Regulation: 8.