ClearanceBrief
510(k) K111334 ยท DQY Catheter, Percutaneous

BENELLI ACCESS DEVICE

ApplicantVascular Solutions, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 1, 2011
ReceivedMay 12, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K111334

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.