ClearanceBrief
510(k) K780321 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

PREGNANCY TEST KIT, OVER-THE-COUNTER

ApplicantIntl. Diagnostic, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 4, 1978
ReceivedFeb 24, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780321

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.