ClearanceBrief
510(k) K073200 ยท DQO Catheter, Intravascular, Diagnostic

GANDRAS INTRAVASCULAR CATHETER, MODELS 5580, 5581 AND 5582

ApplicantVascular Solutions, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Feb 1, 2008
ReceivedNov 13, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073200

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.