ClearanceBrief
510(k) K082933 ยท DQY Catheter, Percutaneous

PASSEO-35 PTA CATHETER

ApplicantBiotronik, Inc., Lake Oswego OR, US
DecisionSubstantially Equivalent, Nov 3, 2008
ReceivedOct 1, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082933

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.