PowerLoc™ Max Power Injectable Infusion Set; SafeStep™ Huber Needle Set

PowerLoc™ Max Power Injectable Infusion Set; SafeStep™ Huber Needle Set is an FDA 510(k)-cleared medical device (K241353) manufactured by Bard Access Systems, 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 November 26, 2024. Regulation: 8.