ClearanceBrief
510(k) K905120 ยท LIO Device, Specimen Collection

SAF FIXATIVE

ApplicantGibson Laboratories, Inc., Lexington KY, US
DecisionSubstantially Equivalent, Dec 17, 1990
ReceivedNov 14, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905120

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.