PORTEX HYPODERMIC NEEDLE-PRO FIXED NEEDLE SYRINGE

PORTEX HYPODERMIC NEEDLE-PRO FIXED NEEDLE SYRINGE is an FDA 510(k)-cleared medical device (K063755) 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 26, 2007. Regulation: 8.