REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER

REPLACEMENT PARTS FOR CPI 6888 LEAD TUNNELER is an FDA 510(k)-cleared medical device (K934727) manufactured by Cardiac Pacemakers, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 9, 1994. Regulation: 8.