ClearanceBrief
510(k) K905499 ยท DQO Catheter, Intravascular, Diagnostic

SCIMD 7 FR. TRIGUIDE GUIDING CATHETER

ApplicantScimed Life Systems, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Feb 11, 1991
ReceivedDec 7, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905499

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.