MANAN HUBER STYLE INFUSION NEEDLE

MANAN HUBER STYLE INFUSION NEEDLE is an FDA 510(k)-cleared medical device (K883744) manufactured by Manan Medical Products, 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 September 27, 1988. Regulation: 8.