ClearanceBrief
510(k) K913364 ยท DQO Catheter, Intravascular, Diagnostic

SCIMED 7 FR. & 8 FR.

ApplicantScimed Life Systems, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Aug 30, 1991
ReceivedJul 29, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913364

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.