ClearanceBrief
510(k) K082030 ยท DLJ Calibrators, Drug Specific

DIMENSION VISTA CSAE CALIBRATOR, MODEL KC440

ApplicantSiemens Healthcare Diagnostics, Inc., Newark DE, US
DecisionSubstantially Equivalent, Aug 22, 2008
ReceivedJul 17, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082030

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.