ClearanceBrief
510(k) K960070 ยท DQO Catheter, Intravascular, Diagnostic

NUMED ATRIOSEPTOSTOMY CATHETER

ApplicantNuMED, Inc., Hopkinton NY, US
DecisionSubstantially Equivalent, Apr 2, 1996
ReceivedJan 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960070

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.