510(k) K240394 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
multiFlux 1000 (F00012408)
| Applicant | Fresenius Medical Care Renal Therapies Group, LLC, Waltham MA, US |
| Decision | Substantially Equivalent, May 31, 2024 |
| Received | Feb 8, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K240394
No recall in the FDA data names this 510(k).
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