B-D ULTRA-FINE II PEN NEEDLE

B-D ULTRA-FINE II PEN NEEDLE is an FDA 510(k)-cleared medical device (K950466) 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 May 10, 1995. Regulation: 8.