KENDALL DUAL LUMEN CATHETER

KENDALL DUAL LUMEN CATHETER is an FDA 510(k)-cleared medical device (K963446) manufactured by Kendall Healthcare Products Co. Div.Of Tyco Health. 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 March 17, 1997. Regulation: 8.