510(k) K910236 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
RENAFLO HDF 1350 HEMODIAFILTER
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 9, 1991 |
| Received | Jan 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910236
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.