ClearanceBrief
510(k) K954610 ยท DTB Permanent Pacemaker Electrode

MODEL 430-07 ENDOCARDIAL PACING LEAD

ApplicantIntermedics, Inc., Angleton TX, US
DecisionSubstantially Equivalent - Subject to Tracking & PMS, Dec 16, 1996
ReceivedOct 4, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954610

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.