510(k) K902149 ยท FKX System, Peritoneal, Automatic Delivery
FRESENIUS/DELMED 90/2 PERITONEAL DIALYSIS SYSTEM
| Applicant | Fresenius/Delmed, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Oct 30, 1990 |
| Received | May 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902149
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.