ClearanceBrief
510(k) K925168 ยท DTD Pacemaker Lead Adaptor

MISCELLANEOUS PACING LEAD

ApplicantOscor Medical Corp., Palm Harbor FL, US
DecisionSubstantially Equivalent, May 3, 1994
ReceivedOct 13, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925168

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.