510(k) K823288 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
AMICON DIAFILTERS 20 & 30 HEMOFILTERS
| Applicant | Amicon, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 16, 1982 |
| Received | Nov 4, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823288
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.