510(k) K801731 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
C-DAK DUO-FLUX ARTIFICIAL KIDNEY
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 13, 1980 |
| Received | Jul 25, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801731
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.