HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE

HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE is an FDA 510(k)-cleared medical device (K073188) manufactured by Smiths Medical Asd, Inc.. 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 February 7, 2008. Regulation: 8.