510(k) K901477 ยท FKX System, Peritoneal, Automatic Delivery
DELMED 80/2 DIALYSIS SYSTEM W/ULTRAFILTRATION
| Applicant | Delmed, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Jul 27, 1990 |
| Received | Mar 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901477
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.