MODIFICATION TO BD ECLIPSE HYPODERMIC NEEDLE

MODIFICATION TO BD ECLIPSE HYPODERMIC NEEDLE is an FDA 510(k)-cleared medical device (K043397) 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 December 28, 2004. Regulation: 8.