BD Alaris™ Pump Epidural Infusion Set

BD Alaris™ Pump Epidural Infusion Set is an FDA 510(k)-cleared medical device (K221319) manufactured by Care Fusion. 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 20, 2023. Regulation: 8.