ClearanceBrief
510(k) K964283 ยท FPB Filter, Infusion Line

AUTOPRIME

ApplicantArbor Technologies, Inc., Ann Arbor MI, US
DecisionSubstantially Equivalent, Jan 22, 1997
ReceivedOct 28, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964283

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.