510(k) K830487 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
HEMO-PROCESSING SYSTEM
| Applicant | Sartorius Filters, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 28, 1983 |
| Received | Feb 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830487
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.