ClearanceBrief
510(k) K843254 ยท LDR Controller, Infusion, Intravascular, Electronic

DK*300 VOLUMETRIC INFUSION CONTROLLER

ApplicantDeka Research & Development Corp., Manchester NH, US
DecisionSubstantially Equivalent, Oct 11, 1984
ReceivedAug 20, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843254

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.