ClearanceBrief
510(k) K001804 ยท DXF Catheter, Septostomy

NUMED Z-5 ATRIOSEPTOSTOMY CATHETER

ApplicantNuMED, Inc., Hopkinton NY, US
DecisionSubstantially Equivalent, Jul 12, 2000
ReceivedJun 15, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K001804

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.