ClearanceBrief
510(k) K842611 ยท IKN Electromyograph, Diagnostic

CA2000

ApplicantNicolet Biomedical Instruments, Mchenry IL, US
DecisionSubstantially Equivalent, Jul 20, 1984
ReceivedJul 5, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842611

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.