510(k) K926373 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ALTRA FLUX 200 HEMODIALYZER
| Applicant | Althin Medical AB an Affiliate of Baxter Intl, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 13, 1995 |
| Received | Dec 22, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926373
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.