REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS

REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS is an FDA 510(k)-cleared medical device (K052603) manufactured by Alliance Medical 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 November 15, 2005. Regulation: 8.