ENDOCARDIAL SCREW-IN LEAD WITH PLATINUM POROUS TIP

ENDOCARDIAL SCREW-IN LEAD WITH PLATINUM POROUS TIP is an FDA 510(k)-cleared medical device (K852446) manufactured by Diag Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 16, 1985. Regulation: 8.