VASCULAR ACCESS PORT HUBER POINT INFUSION NEEDLES

VASCULAR ACCESS PORT HUBER POINT INFUSION NEEDLES is an FDA 510(k)-cleared medical device (K884792) manufactured by Infucare 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 January 29, 1989. Regulation: 8.