ClearanceBrief
510(k) K955903 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

SELFCARE EARLY PREGNANCY TEST

ApplicantCambridge Diagnostics Ireland, Ltd., Galway, IE
DecisionSubstantially Equivalent, Mar 6, 1996
ReceivedDec 29, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955903

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.