510(k) K220281 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
multiFiltratePRO System
| Applicant | Fresenius Medical Care Renal Therapies Group, LLC, Waltham MA, US |
| Decision | Substantially Equivalent, Dec 16, 2022 |
| Received | Feb 1, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220281
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.