ClearanceBrief
510(k) K933794 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

ANI BIOCARD(TM) HCG TEST

ApplicantCanadian Bioclinical, Ltd., Ontario, Canada, CA
DecisionSubstantially Equivalent, May 19, 1994
ReceivedAug 4, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933794

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.