ClearanceBrief
510(k) K874258 ยท JHI Visual, Pregnancy Hcg, Prescription Use

VENTRESCREEN, HCG URINE

ApplicantVentrex Laboratories, Inc., Portland ME, US
DecisionSubstantially Equivalent, Nov 23, 1987
ReceivedOct 20, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874258

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.