ClearanceBrief
510(k) K052112 ยท IKN Electromyograph, Diagnostic

XLTEK XCALIBUR EMG / LT, MODEL PK1P33, PK1059

ApplicantExcel Tech. , Ltd., Oakville, CA
DecisionSubstantially Equivalent, Oct 28, 2005
ReceivedAug 4, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K052112

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.