ClearanceBrief
510(k) K120381 ยท DQY Catheter, Percutaneous

Q50 PLUS STENT GRAFT BALLOON CATHETER

ApplicantQxmedical, LLC, St. Paul MN, US
DecisionSubstantially Equivalent, Feb 24, 2012
ReceivedFeb 7, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120381

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.