ClearanceBrief
510(k) K171136 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

LIA Pregnancy Test

ApplicantLia Diagnostics, Philadelphia PA, US
DecisionSubstantially Equivalent, Nov 20, 2017
ReceivedApr 17, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171136

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.