510(k) K852251 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FRESENIUS HEMOFLOW F60 & FRESENIUS HEMOFLOW F40
| Applicant | Seratronics, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Jul 25, 1985 |
| Received | May 23, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852251
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.