LIFELINE TLE J-SHAPED ATRIAL ENDOCARDIAL

LIFELINE TLE J-SHAPED ATRIAL ENDOCARDIAL is an FDA 510(k)-cleared medical device (K792301) manufactured by Intermedics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 3, 1980. Regulation: 8.