CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set

CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set is an FDA 510(k)-cleared medical device (K193380) manufactured by Codman & Shurtleff, 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 July 19, 2020. Regulation: 8.