ClearanceBrief
510(k) K024190 ยท FRN Pump, Infusion

FENESTRATED INFUSION CATHETER

ApplicantPromedic, Inc., Mccordsville IN, US
DecisionSubstantially Equivalent, Mar 17, 2003
ReceivedDec 19, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K024190

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.