ClearanceBrief
510(k) K082559 ยท DQY Catheter, Percutaneous

SPECTRANETICS CROSS-PILOT TURBO ELITE SUPPORT CATHETER

ApplicantSpectranetics Corp., Colorado Springs CO, US
DecisionSubstantially Equivalent, Dec 11, 2008
ReceivedSep 4, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082559

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.