ClearanceBrief
510(k) K972419 ยท IKN Electromyograph, Diagnostic

TOENNIES NEUROSCREEN SYSTEM

ApplicantErich Jaeger, Inc., Hoechberg, Germany, DE
DecisionSubstantially Equivalent, Apr 30, 1998
ReceivedJun 27, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972419

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.