ClearanceBrief
510(k) K781399 ยท IKN Electromyograph, Diagnostic

TECA MODEL B9 ELECTROMYOGRAPH

ApplicantTeca, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 20, 1978
ReceivedAug 15, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781399

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.