510(k) K141051 ยท MSD Catheter, Hemodialysis, Implanted
VECTORFLOW; ANTEGRADE CHRONIC HEMODIALYSIS CATHETER, RETROGRADE CHRONIC HEMODIALYSIS CATHETER, RETROGRADE REPLACEMENT HU
| Applicant | Arrow International, Inc., Reading PA, US |
| Decision | Substantially Equivalent, Jul 7, 2014 |
| Received | Apr 24, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141051
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 13, 2026 | ARROW INTERNATIONAL, LLC Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15192-VFI, CS-15192-VFIE, CS-15232-VFI, CS-15232-VFIE, CS-15272-VFI, CS-15272-VFIE, Open, Classified |
MSD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.