ClearanceBrief
510(k) K821237 ยท IKN Electromyograph, Diagnostic

NEUROMATIC 2000

ApplicantDisa Electronics, Walker MI, US
DecisionSubstantially Equivalent, May 21, 1982
ReceivedApr 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821237

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.