ClearanceBrief
510(k) K936287 ยท JHI Visual, Pregnancy Hcg, Prescription Use

KODAK SURECELL HCG URINE TEST, MODIFICATION

ApplicantEastman Kodak Company, Rochester NY, US
DecisionSubstantially Equivalent, Apr 8, 1994
ReceivedDec 23, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K936287

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.