ClearanceBrief
510(k) K915727 ยท CKG Radioimmunoassay, Acth

ACTH IRMA KIT II MITSUBISHI YUKA

ApplicantMitsubishi Yuka America, Inc., Washington DC, US
DecisionSubstantially Equivalent, Mar 2, 1992
ReceivedDec 20, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915727

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.