Anchor Dual Lumen Guidewire Catheter

Anchor Dual Lumen Guidewire Catheter is an FDA 510(k)-cleared medical device (K201076) manufactured by Aqure Medical, 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 August 5, 2020. Regulation: 8.