510(k) K844790 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
RENAFLO HEMOCONCENTRATOR
| Applicant | Renal Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 23, 1985 |
| Received | Dec 10, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844790
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.