ClearanceBrief
510(k) K872836 ยท IKN Electromyograph, Diagnostic

SPINOSCOPE

ApplicantDiagnospine Fabrication, Inc., Canada H3h 1e8, CA
DecisionSubstantially Equivalent, Sep 29, 1987
ReceivedJul 17, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872836

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.