AUTOLANCET

AUTOLANCET is an FDA 510(k)-cleared medical device (K822209) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 1982. Regulation: 8.