DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS is an FDA 510(k)-cleared medical device (K930286) manufactured by Concord/Portex. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 21, 1993. Regulation: 8.