MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR

MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR is an FDA 510(k)-cleared medical device (K000087) manufactured by The Kendal Co.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 16, 2000. Regulation: 8.