VIDAPORT INTRAOSSEOUS INFUSION SYSTEM

VIDAPORT INTRAOSSEOUS INFUSION SYSTEM is an FDA 510(k)-cleared medical device (K032885) manufactured by Vidacare Corporation. 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 March 9, 2004. Regulation: 8.