510(k) K000028 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
RENAFLO II HF 2000 HEMOFILTER
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 4, 2000 |
| Received | Jan 5, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000028
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.