ClearanceBrief
510(k) K890134 ยท LIO Device, Specimen Collection

FTK FECAL TRANSPORT KIT

ApplicantEvergreen Scientific, Inc., Los Angeles CA, US
DecisionSubstantially Equivalent, Apr 21, 1989
ReceivedJan 13, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890134

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.