ClearanceBrief
510(k) K801172 ยท DTB Permanent Pacemaker Electrode

INTERMEDICS' LIFELINE TLE ENDOCARDIAL

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 1, 1980
ReceivedMay 16, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801172

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.