ClearanceBrief
510(k) K882345 ยท DTB Permanent Pacemaker Electrode

PERMANENT PACING LEADS PYBJ SERIES

ApplicantOscor Medical Corp., Palm Harbor FL, US
DecisionSubstantially Equivalent, Oct 28, 1988
ReceivedJun 7, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882345

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.