ClearanceBrief
510(k) K040866 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

FIRST RESPONSE ONE-STEP DIGITAL PREGNANCY TEST

ApplicantArmkel, LLC, Princeton NJ, US
DecisionSubstantially Equivalent, Oct 19, 2004
ReceivedApr 2, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040866

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.