PACESETTER SYS FAST PASS ENDOCARDIAL LEAD 856 INLI

PACESETTER SYS FAST PASS ENDOCARDIAL LEAD 856 INLI is an FDA 510(k)-cleared medical device (K853914) manufactured by Pacesetter Systems. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 2, 1985. Regulation: 8.