ClearanceBrief
510(k) K990138 ยท LOJ Kit, Test,Alpha-Fetoprotein For Testicular Cancer

DSL ACTIVE AFP ELISA, MODEL DSL-10-8400

ApplicantDiagnostic Systems Laboratories, Inc., Webster TX, US
DecisionSubstantially Equivalent, Jun 21, 1999
ReceivedJan 19, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990138

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.