Arrow Pressure Injectable Midline Catheter

Arrow Pressure Injectable Midline Catheter is an FDA 510(k)-cleared medical device (K213855) manufactured by Arrow International, LLC Subsidiary of Teleflex Incorporated. 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 September 1, 2022. Regulation: 8.