EkoSonic Endovascular Device, EKOS+ Endovascular Device

EkoSonic Endovascular Device, EKOS+ Endovascular Device is an FDA 510(k)-cleared medical device (K213422) manufactured by Boston Scientific Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 13, 2021. Regulation: 8.