510(k) K861106 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FRESENIUS HEMOFLOW F80 DIALYZER
| Applicant | Seratronics, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Apr 7, 1986 |
| Received | Mar 24, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861106
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.