ClearanceBrief
510(k) K092702 ยท DQO Catheter, Intravascular, Diagnostic

MICRUS MICROCATHETER, MODEL COURIER 270

ApplicantMicrus Endovascular Corporation, San Jose CA, US
DecisionSubstantially Equivalent, Nov 20, 2009
ReceivedSep 2, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K092702

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.