ClearanceBrief
510(k) K900147 ยท CKG Radioimmunoassay, Acth

MODIFIED DSL-2300 ACTH RIA

ApplicantDiagnostic Systems Laboratories, Inc., Webster TX, US
DecisionSubstantially Equivalent, Mar 1, 1990
ReceivedJan 11, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900147

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.