ClearanceBrief
510(k) K160662 ยท DQO Catheter, Intravascular, Diagnostic

Surefire Infusion System

ApplicantSurefire Medical, Inc., Westminster CO, US
DecisionSubstantially Equivalent, Mar 11, 2016
ReceivedMar 9, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K160662

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.