DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.

DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD. is an FDA 510(k)-cleared medical device (K905311) 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.