ClearanceBrief
510(k) K860333 ยท CEP Radioimmunoassay, Luteinizing Hormone

MICRO-ELISA HLH TEST KIT MONOCLONAL

ApplicantBioclinical Systems, Inc., St.Louis MO, US
DecisionSubstantially Equivalent, Apr 21, 1986
ReceivedJan 29, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860333

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.