510(k) K260533 · KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ELISIO-H
| Applicant | Nipro Medical Corporation, Miami FL, US |
| Decision | Substantially Equivalent, Mar 19, 2026 |
| Received | Feb 17, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K260533
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.