ClearanceBrief
510(k) K901566 ยท IKK System, Isokinetic Testing And Evaluation

PROMATRON 3000

ApplicantPromatek Medical Systems, Inc., Joliet IL, US
DecisionSubstantially Equivalent, Oct 29, 1990
ReceivedApr 3, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901566

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.