THE TULIP COMPANY BRANSON OVERSHEATH

THE TULIP COMPANY BRANSON OVERSHEATH is an FDA 510(k)-cleared medical device (K952958) 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 November 13, 1995. Regulation: 8.