ClearanceBrief
510(k) K791235 ยท IKN Electromyograph, Diagnostic

CADWELL 7000 ELECTROMYOGRAPH MACHINE

ApplicantCadwell Laboratories, Inc., Walker MI, US
DecisionSubstantially Equivalent, Aug 16, 1979
ReceivedJul 6, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791235

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.