ClearanceBrief
510(k) K880472 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

ADVANCE* AND DAISY* PREGNANCY TEST

ApplicantAdvanced Care Products, Raritan NJ, US
DecisionSubstantially Equivalent, May 16, 1988
ReceivedFeb 4, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880472

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.