ClearanceBrief
510(k) K790664 ยท IKN Electromyograph, Diagnostic

MODEL 1309 AUDIO MONITOR

ApplicantLife-Tech Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 23, 1979
ReceivedApr 6, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790664

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.