ClearanceBrief
510(k) K922042 ยท DTB Permanent Pacemaker Electrode

CARDIFIX ENDOCARDIAL PACING LEAD

ApplicantIntermedics, Inc., Angleton TX, US
DecisionUnknown, Apr 29, 1993
ReceivedMay 1, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922042

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.