CARDIOPULMONARY BYPASS PUMP TUBING

CARDIOPULMONARY BYPASS PUMP TUBING is an FDA 510(k)-cleared medical device (K801394) manufactured by Texas Medical Products, 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 June 29, 1980. Regulation: 8.