ClearanceBrief
510(k) K902136 ยท JHI Visual, Pregnancy Hcg, Prescription Use

KODAK SURECELL(TM) HCG-URINE TEST KIT

ApplicantEastman Kodak Company, Rochester NY, US
DecisionSubstantially Equivalent, Jun 28, 1990
ReceivedMay 10, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902136

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.