ClearanceBrief
510(k) K910987 ยท DQO Catheter, Intravascular, Diagnostic

7FR. AND 8FR. TRIGUIDE GUIDING CATHETER ADD. CURVE

ApplicantScimed, Minneapolis MN, US
DecisionSubstantially Equivalent, May 29, 1991
ReceivedMar 7, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910987

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.