510(k) K840449 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
AMICON DIAFILTER 40. HEMOFILTER
| Applicant | Medical Device Consultants, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Mar 23, 1984 |
| Received | Feb 1, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840449
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.