ClearanceBrief
510(k) K160482 ยท LZG Pump, Infusion, Insulin

t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater

ApplicantTandem Diabetes Care, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jul 13, 2016
ReceivedFeb 22, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160482

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.