ClearanceBrief
510(k) K130220 ยท GXZ Electrode, Needle

MR CONDITIONAL PRESSON ELECTRODE

ApplicantRhythmlink International, LLC, Columbia SC, US
DecisionSubstantially Equivalent, Jul 22, 2013
ReceivedJan 29, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130220

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.