PowerGlide Pro™ Midline Catheter

PowerGlide Pro™ Midline Catheter is an FDA 510(k)-cleared medical device (K240359) manufactured by Becton, Dickinson and Company (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 July 28, 2024. Regulation: 8.