ClearanceBrief
510(k) K001145 ยท GKP Instrument, Coagulation, Automated

SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000

ApplicantDade Behring, Inc., Miami FL, US
DecisionSubstantially Equivalent, May 11, 2000
ReceivedApr 10, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001145

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.