Medline Reinforced Epidural Catheter

Medline Reinforced Epidural Catheter is an FDA 510(k)-cleared medical device (K181782) manufactured by Medline Industries, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 3, 2019. Regulation: 8.