ClearanceBrief
510(k) K003085 ยท DQY Catheter, Percutaneous

CONCENTRIC GUIDE CATHETER, MODELS 90018, 90020

ApplicantConcentric Medical, Inc., Moutian View CA, US
DecisionSubstantially Equivalent, Mar 7, 2001
ReceivedOct 3, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003085

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.