CerusEndo Microcatheter (027)

CerusEndo Microcatheter (027) is an FDA 510(k)-cleared medical device (K213314) manufactured by Cerus Endovascular, 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 March 14, 2022. Regulation: 8.