ClearanceBrief
510(k) K070372 ยท DQY Catheter, Percutaneous

GOPHER 2F SUPPORT CATHETER, MODEL 5600 AND GOPHER 3F SUPPORT CATHETER, MODEL 5610

ApplicantVascular Solutions, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jun 1, 2007
ReceivedFeb 8, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070372

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.