THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION)

THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION) is an FDA 510(k)-cleared medical device (K954734) 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.