510(k) K830596 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ULTRAFILTRATION MONITOR UFM-10-2
| Applicant | Gambro, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 27, 1983 |
| Received | Feb 24, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830596
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.