ClearanceBrief
510(k) K091386 ยท FRN Pump, Infusion

MICROFUSE DUAL RATE INFUSER

ApplicantNumia Medical Technology, LLC, Lyndonville VT, US
DecisionSubstantially Equivalent, Oct 2, 2009
ReceivedMay 11, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K091386

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.