510(k) K892262 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FRESENIUS HEMOFLOW, F40M, F50M, F60M & F80M
| Applicant | Fresenius USA, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Apr 25, 1989 |
| Received | Apr 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892262
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.