BD ECLIPSE BIFURCATED NEEDLE

BD ECLIPSE BIFURCATED NEEDLE is an FDA 510(k)-cleared medical device (K032528) 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 September 8, 2003. Regulation: 8.