DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELS

DURAFLO II HEPARIN TREATED FEMORAL CANNULAE MODELS is an FDA 510(k)-cleared medical device (K905312) manufactured by Baxter Bentley Laboratories, 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 January 14, 1991. Regulation: 8.