510(k) K840680 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
CENTRY 2000 DIALYSIS CONTROL UNIT
| Applicant | Cobe Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 20, 1984 |
| Received | Feb 15, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840680
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.