BARD-PARKER OCCLUSION BALLOON CATHETER

BARD-PARKER OCCLUSION BALLOON CATHETER is an FDA 510(k)-cleared medical device (K852294) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 16, 1985. Regulation: 8.