510(k) K895405 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
AMICON MINIFILTER PLUS HEMOFILTER
| Applicant | Amicon, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Jan 11, 1990 |
| Received | Sep 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895405
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.