ClearanceBrief
510(k) K860492 ยท FRN Pump, Infusion

NORDISK INFUSER SYSTEM WITH PRE-FILLED CARTRIDGE

ApplicantNordisk Infuser System, Washington DC, US
DecisionSubstantially Equivalent, Feb 19, 1986
ReceivedFeb 3, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860492

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.