ClearanceBrief
510(k) K932542 ยท DQO Catheter, Intravascular, Diagnostic

SCIMED 6F ANGIOGRAPHIC CATHETER

ApplicantScimed Life Systems, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Aug 11, 1993
ReceivedMay 26, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932542

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.