ClearanceBrief
510(k) K832593 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

HOSPITAL LAB IN-HOME EARLY PREG TEST

ApplicantAicl-Pack, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 11, 1984
ReceivedAug 2, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832593

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.