REPAIR KIT QUINTON TRIPLE LUMEN RIGHT ATRIAL CATHE

REPAIR KIT QUINTON TRIPLE LUMEN RIGHT ATRIAL CATHE is an FDA 510(k)-cleared medical device (K853860) manufactured by Quinton, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 17, 1985. Regulation: 8.