ClearanceBrief
510(k) K042280 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

FACT PLUS ONE-STEP PREGNANCY TEST KIT

ApplicantUnipath , Ltd., Bedford, GB
DecisionSubstantially Equivalent, Sep 10, 2004
ReceivedAug 23, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K042280

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.