510(k) K111900 ยท MSD Catheter, Hemodialysis, Implanted
NEXTSTEP ANTEGRADE CHRONIC HEMODIALYSIS CATHETER
| Applicant | Teleflexmedical, Inc., Reading PA, US |
| Decision | Unknown, Aug 17, 2011 |
| Received | Jul 5, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111900
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 13, 2026 | ARROW INTERNATIONAL, LLC NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-15232-SFX, CS-15272-SFX, CS-15312-SFX, CS-15422-SFX, CS-15502-SFX;
NextStep Antegrade Hemodialysi Open, Classified |
MSD | None listed |
| Jan 22, 2015 | Arrow International Inc The Arrow Edge Hemodialysis Catheterization Set Long-Term Access and NextStep Antegrade Hemodialysis Catheterization Set, Long-Term Access, part numbers: AC-15192-SFX, AC-15232-SFX, AC-15272-SFX, AC-1 Terminated |
MSD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.