ClearanceBrief
510(k) K021409 ยท CEP Radioimmunoassay, Luteinizing Hormone

AT HOME OVULATION TEST, MODEL 9032

ApplicantPhamatech, Inc., San Diego CA, US
DecisionSubstantially Equivalent, May 24, 2002
ReceivedMay 3, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K021409

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.