ClearanceBrief
510(k) K883814 ยท CEP Radioimmunoassay, Luteinizing Hormone

DELFIA HLH SPEC KIT

ApplicantPharmacia, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Mar 8, 1989
ReceivedSep 8, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883814

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.