IMPLANT PROGRAM CARDIAC PULSE GEN W/MOD SET SCREW

IMPLANT PROGRAM CARDIAC PULSE GEN W/MOD SET SCREW is an FDA 510(k)-cleared medical device (K853206) manufactured by Telectronics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 11, 1985. Regulation: 8.