ClearanceBrief
510(k) K813272 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

A-1 IN-HOME PREGNANCY TEST

ApplicantC.F. Medical, Inc., Walker MI, US
DecisionSubstantially Equivalent, Dec 17, 1981
ReceivedNov 20, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813272

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.