VENOUS RESERVOIR BAG MODEL NO. BMR-800 W/HEPARIN

VENOUS RESERVOIR BAG MODEL NO. BMR-800 W/HEPARIN is an FDA 510(k)-cleared medical device (K896414) 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 January 30, 1990. Regulation: 8.