LIVESIRE ELECTROPHYSIOLOGY CATHETER

LIVESIRE ELECTROPHYSIOLOGY CATHETER is an FDA 510(k)-cleared medical device (K022380) manufactured by St Jude Medical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 30, 2002. Regulation: 8.