MAHURKAR TRIPLE LUMEN CATHETER, 12 FR

MAHURKAR TRIPLE LUMEN CATHETER, 12 FR is an FDA 510(k)-cleared medical device (K020089) 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 April 9, 2002. Regulation: 8.