ClearanceBrief
510(k) K880758 ยท CEP Radioimmunoassay, Luteinizing Hormone

SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY

ApplicantBoots-Celltech Diagnostics, Inc., Berkshire, England, GB
DecisionSubstantially Equivalent, Apr 18, 1988
ReceivedFeb 25, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880758

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.