ClearanceBrief
510(k) K940637 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

PREDICTOR HOME PREGNANCY TEST

ApplicantOrganon Teknika Corp., Durham NC, US
DecisionSubstantially Equivalent, Jun 2, 1994
ReceivedFeb 14, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940637

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.