LILY MULTICANNULA GUIDE

LILY MULTICANNULA GUIDE is an FDA 510(k)-cleared medical device (K954999) manufactured by Lily Imaging Solutions 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 April 3, 1996. Regulation: 8.