ClearanceBrief
510(k) K850576 ยท DTD Pacemaker Lead Adaptor

PACESETTER SYS, ENDOCARDIAL, VENTRICULAR, BIPOLAR

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, Mar 6, 1985
ReceivedFeb 13, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850576

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.