BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES

BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES is an FDA 510(k)-cleared medical device (K001390) manufactured by Biosense Webster, 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 20, 2000. Regulation: 8.