RESPIRATORY EXERCISOR, VOLUME PULSE

RESPIRATORY EXERCISOR, VOLUME PULSE is an FDA 510(k)-cleared medical device (K781669) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 22, 1978. Regulation: 8.