EXTRACORPOREAL CIRCUIT W/DURAFLO II HEPARIN TREATM

EXTRACORPOREAL CIRCUIT W/DURAFLO II HEPARIN TREATM is an FDA 510(k)-cleared medical device (K932208) manufactured by Baxter Healthcare Corp. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 8, 1994. Regulation: 8.