ANGIOCATH AUTOGUARD CATHETER, INSYTE AUTOGUARD CATHETER

ANGIOCATH AUTOGUARD CATHETER, INSYTE AUTOGUARD CATHETER is an FDA 510(k)-cleared medical device (K984059) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. 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 April 8, 1999. Regulation: 8.