ClearanceBrief
510(k) K030533 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

ACCUNATE ONE-STEP,ACCUNATE ONE-STEP CASSETTE, ACCUNATE-CHOICE, ACCUNATE HOME PREGNANCY TEST

ApplicantCenogenics Corp., Morganville NJ, US
DecisionSubstantially Equivalent, Apr 17, 2003
ReceivedFeb 14, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030533

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.