ClearanceBrief
510(k) K954551 ยท DTB Permanent Pacemaker Electrode

DF-1 TERMINAL CAP

ApplicantPacesetter, Inc., Sylmar CA, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Dec 26, 1995
ReceivedOct 2, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954551

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.