CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.

CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL. is an FDA 510(k)-cleared medical device (K880103) manufactured by Research Medical, 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 March 21, 1988. Regulation: 8.