ClearanceBrief
510(k) K930694 ยท DQO Catheter, Intravascular, Diagnostic

MEDI-DYNE ANGIOGRAPHIC CATHETER

ApplicantMedi-Dyne, Inc., Glens Falls NY, US
DecisionSubstantially Equivalent, Aug 2, 1993
ReceivedFeb 10, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930694

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.