ClearanceBrief
510(k) K840174 ยท CEP Radioimmunoassay, Luteinizing Hormone

LH QUIK RIA KIT

ApplicantPacific Biotech, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 19, 1984
ReceivedJan 17, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840174

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.