ClearanceBrief
510(k) K991059 ยท DQY Catheter, Percutaneous

SPECTRANETICS 0.014 SUPPORT CATHETER, MODEL 518-016, SPECTRANETICS 0.018 SUPPORT CATHETER, MODEL 518-017

ApplicantSpectranetics Corp., Colorado Springs CO, US
DecisionSubstantially Equivalent, Nov 16, 1999
ReceivedMar 30, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991059

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.