ClearanceBrief
510(k) K950731 ยท DQO Catheter, Intravascular, Diagnostic

SCIMED 6 FRENCH EXPO ANGIOGRAPHIC CATHETER

ApplicantScimed Life Systems, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Apr 5, 1995
ReceivedFeb 16, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950731

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.