ClearanceBrief
510(k) K903429 ยท IKK System, Isokinetic Testing And Evaluation

LIDO LINEA

ApplicantLoredan Biomedical, Inc., Davis CA, US
DecisionSubstantially Equivalent, Aug 14, 1990
ReceivedJul 31, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903429

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.