OASIS THROMBECTOMY CATHETER SYSTEM

OASIS THROMBECTOMY CATHETER SYSTEM is an FDA 510(k)-cleared medical device (K982363) manufactured by Boston Scientific Corp. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 22, 1999. Regulation: 8.