ClearanceBrief
510(k) K813152 ยท DTD Pacemaker Lead Adaptor

ELECTRODE TERMINAL CAP

ApplicantPacesetter Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Dec 2, 1981
ReceivedNov 6, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813152

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.