510(k) K873887 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
MODIFIED HOLLOW FIBERS USED IN DIAFILTER HEMOFIL.
| Applicant | W.R. Grace & Co.-Conn., Danvers MA, US |
| Decision | Substantially Equivalent, Dec 9, 1987 |
| Received | Sep 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873887
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.