ClearanceBrief
510(k) K101806 ยท MRZ Accessories, Pump, Infusion

AIDERA DIASEND SYSTEM

ApplicantAidera AB, Goteborg, SE
DecisionSubstantially Equivalent, Dec 7, 2010
ReceivedJun 28, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101806

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.