KIM NASO-INTESTINAL TUBE

KIM NASO-INTESTINAL TUBE is an FDA 510(k)-cleared medical device (K882918) manufactured by Sheridan Catheter Corp.. 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 December 4, 1988. Regulation: 8.