Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020)

Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020) is an FDA 510(k)-cleared medical device (K251185) manufactured by Intervene. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 21, 2025. Regulation: 8.