ClearanceBrief
510(k) K140307 ยท DQY Catheter, Percutaneous

ENVOY GUIDING CATHETER

ApplicantCodman & Shurtleff, Inc., Raynham MA, US
DecisionSubstantially Equivalent, Apr 21, 2014
ReceivedFeb 7, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K140307

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.