SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023

SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 is an FDA 510(k)-cleared medical device (K041453) manufactured by Smith & Nephew, 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 21, 2004. Regulation: 8.