CARDIOPULMONARY BYPASS VASCULAR CATHETER

CARDIOPULMONARY BYPASS VASCULAR CATHETER is an FDA 510(k)-cleared medical device (K905224) manufactured by 3M Health Care, Sarns. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 4, 1991. Regulation: 8.