ClearanceBrief
510(k) K250930 ยท QFG Alternate Controller Enabled Insulin Infusion Pump

twiist system

ApplicantDeka Research & Development Corp., Manchester NH, US
DecisionSubstantially Equivalent, Apr 2, 2025
ReceivedMar 28, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K250930

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.