MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE

MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE is an FDA 510(k)-cleared medical device (K031200) manufactured by Becton, Dickinson & CO. 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 June 23, 2003. Regulation: 8.