ClearanceBrief
510(k) K860542 ยท JHI Visual, Pregnancy Hcg, Prescription Use

TANDEM ICON II HCG IMMUNOENZYMETRIC ASSAY KIT

ApplicantHybritech, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Mar 5, 1986
ReceivedFeb 12, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860542

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.