DAIG DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER

DAIG DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER is an FDA 510(k)-cleared medical device (K942379) manufactured by Daig 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 December 26, 1994. Regulation: 8.