ClearanceBrief
510(k) K970082 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

ABBOTT ADVISOR ONE-STEP PREGNANCY TEST

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, Jan 24, 1997
ReceivedJan 9, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970082

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.