ClearanceBrief
510(k) K021241 ยท GKZ Counter, Differential Cell

SYSMEX XT-SERIES, MODEL XT-2000I AND XT-1800I

ApplicantSysmex Corporation of America, Long Grove IL, US
DecisionSubstantially Equivalent, Jun 25, 2002
ReceivedApr 19, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021241

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.