ClearanceBrief
510(k) K162383 ยท IKN Electromyograph, Diagnostic

Cadwell Sierra Summit, Cadwell Sierra Ascent

ApplicantCadwell Industries, Inc., Kennewick WA, US
DecisionSubstantially Equivalent, Mar 1, 2017
ReceivedAug 25, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K162383

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.