VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES

VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES is an FDA 510(k)-cleared medical device (K061483) manufactured by Greiner Bio-One North America, 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 August 13, 2006. Regulation: 8.