ClearanceBrief
510(k) K023114 ยท PDU Catheter For Crossing Total Occlusions

LUMEND FRONTRUNNER CTO CATHETER

ApplicantLumend, Inc., Redwood City CA, US
DecisionSubstantially Equivalent, Jan 23, 2003
ReceivedSep 19, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023114

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.