ClearanceBrief
510(k) K093184 ยท DQY Catheter, Percutaneous

ENVOY GUIDING CATHETERS

ApplicantCodman & Shurtleff, Inc., Raynham MA, US
DecisionSubstantially Equivalent, Nov 6, 2009
ReceivedOct 9, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093184

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.