KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER

KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER is an FDA 510(k)-cleared medical device (K002901) manufactured by The Kendall Company. 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 27, 2001. Regulation: 8.