ClearanceBrief
510(k) K032069 ยท DQY Catheter, Percutaneous

WORKHORSE II PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY BALLOON CATHETER

ApplicantAngioDynamics, Inc., Queensburgy NY, US
DecisionSubstantially Equivalent, Aug 27, 2003
ReceivedJul 3, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032069

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.