ClearanceBrief
510(k) K883279 ยท CGJ Radioimmunoassay, Follicle-Stimulating Hormone

PHASE II FSH KIT

ApplicantVitek Systems, Inc., Rockland MA, US
DecisionSubstantially Equivalent, Sep 9, 1988
ReceivedAug 3, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883279

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.