ClearanceBrief
510(k) K151234 ยท DQX Wire, Guide, Catheter

R350 guidewire

ApplicantVascular Solutions, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Nov 18, 2015
ReceivedMay 8, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151234

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.