510(k) K884353 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ULTRX(TM) 850 ARTIFICIAL KIDNEY
| Applicant | Cd Medical, Inc., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Dec 8, 1988 |
| Received | Oct 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884353
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.