ClearanceBrief
510(k) K123746 ยท IKK System, Isokinetic Testing And Evaluation

AMES THERAPY DEVICE

ApplicantAmes Technology, Inc., Eugene OR, US
DecisionSubstantially Equivalent, May 24, 2013
ReceivedDec 6, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123746

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.