AXILLARY BLOCK NEEDLE

AXILLARY BLOCK NEEDLE is an FDA 510(k)-cleared medical device (K880970) 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 April 20, 1988. Regulation: 8.