ClearanceBrief
510(k) K921318 ยท DTD Pacemaker Lead Adaptor

ADAPTING SLEEVE KIT MODEL 4023

ApplicantSiemens-Pacesetter, Inc., Sylmar CA, US
DecisionSubstantially Equivalent, Aug 3, 1992
ReceivedMar 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921318

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.