ClearanceBrief
510(k) K131931 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

CHEMTRUE(R) HCG PREGNANCY URINE MIDSTREAM TEST

ApplicantChemtron Biotech, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jul 26, 2013
ReceivedJun 27, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131931

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.