510(k) K880459 ยท FKP System, Dialysate Delivery, Single Patient
480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE
| Applicant | Cd Medical, Inc., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Apr 13, 1988 |
| Received | Feb 3, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880459
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.