ClearanceBrief
510(k) K821944 ยท JHI Visual, Pregnancy Hcg, Prescription Use

TANDEM HCG IMMUNOEZYMETRIC ASSAY KIT

ApplicantHybritech, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 22, 1982
ReceivedJun 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821944

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.