ClearanceBrief
510(k) K191275 · LIT Catheter, Angioplasty, Peripheral, Transluminal

All’InCath 035M PTA Balloon Dilatation Catheter

ApplicantNexstep Medical, Dijon, FR
DecisionSubstantially Equivalent, Jan 15, 2020
ReceivedMay 13, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191275

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.