ClearanceBrief
510(k) K091596 ยท DRA Catheter, Steerable

EVALVE STEERABLE GUIDE CATHETER, MODEL SGC01ST

ApplicantEvalve, Inc., Menlo Park CA, US
DecisionSubstantially Equivalent, Jul 2, 2009
ReceivedJun 2, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K091596

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.