ClearanceBrief
510(k) K942059 ยท LYH Arthrometer

KT2000 KNEE LIGAMENT ARTHROMETER

ApplicantMedmetric Corp., San Diego CA, US
DecisionSubstantially Equivalent, Sep 20, 1994
ReceivedApr 29, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942059

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.