ClearanceBrief
510(k) K890844 ยท CAK Microfilter, Blood Transfusion

MICROSEPT 60/20

ApplicantArbor Technologies, Inc., Ann Arbor MI, US
DecisionSubstantially Equivalent, Jun 7, 1989
ReceivedFeb 21, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890844

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.