510(k) K863823 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
AMICON DIAFILTER HEMOFILTER
| Applicant | Amicon, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Nov 6, 1986 |
| Received | Sep 30, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863823
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.