HUBER NEEDLE INFUSION SET MODEL #20G01 & Y-SITE MODEL #20G01Y

HUBER NEEDLE INFUSION SET MODEL #20G01 & Y-SITE MODEL #20G01Y is an FDA 510(k)-cleared medical device (K981683) manufactured by Venusa , Ltd.. 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 July 27, 1998. Regulation: 8.