ClearanceBrief
510(k) K940545 ยท DQY Catheter, Percutaneous

SCIMED 10 FR LARGE LUMEN TRIGUIDE-FLEX GUID CATH

ApplicantScimed Life Systems, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, May 6, 1994
ReceivedFeb 7, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940545

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.