BARD PARKER THORACIC VENT

BARD PARKER THORACIC VENT is an FDA 510(k)-cleared medical device (K854634) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 26, 1985. Regulation: 8.