ClearanceBrief
510(k) K812806 ยท LYH Arthrometer

KT-1000 DEVICE

ApplicantMedmetric Corp. MD, US
DecisionSubstantially Equivalent, Nov 10, 1981
ReceivedOct 6, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812806

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.