ClearanceBrief
510(k) K011660 ยท LDF Electrode, Pacemaker, Temporary

WECK CARDIAC PACING WIRES

ApplicantWeck Closure Systems, Research Triangle Park NC, US
DecisionSubstantially Equivalent, Aug 21, 2001
ReceivedMay 29, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011660

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.