Liberant™ RX Aspiration Catheter

Liberant™ RX Aspiration Catheter is an FDA 510(k)-cleared medical device (K253589) manufactured by Medtronic Interventional Vascular, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 22, 2026. Regulation: 8.