ClearanceBrief
510(k) K021032 ยท CKG Radioimmunoassay, Acth

ACTH IMMUNORADIOMETRIC (IRMA) DIAGNOSTIC ASSAY KIT, MODEL #3KG100

ApplicantScantibodies Laboratory, Inc., Santee CA, US
DecisionSubstantially Equivalent, Jun 3, 2002
ReceivedMar 29, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021032

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.