ClearanceBrief
510(k) K030258 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

FIRST RESPONSE PREGNANCY TEST

ApplicantArmkel, LLC, Princeton NJ, US
DecisionSubstantially Equivalent, Feb 25, 2003
ReceivedJan 24, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030258

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.