ClearanceBrief
510(k) K091703 ยท QEZ Aspiration Thrombectomy Catheter

HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131

ApplicantConcentric Medical, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Oct 14, 2009
ReceivedJun 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091703

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.