ClearanceBrief
510(k) K073700 ยท DQY Catheter, Percutaneous

6F PROXIS SYSTEM

ApplicantSt. Jude Medical, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Oct 2, 2008
ReceivedDec 31, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073700

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.