510(k) K023874 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
SYSTEM 100 ULTRAFILTRATION CATHETER
| Applicant | Chf Solutions, Inc., Brooklyn Park MN, US |
| Decision | Substantially Equivalent, Nov 20, 2003 |
| Received | Nov 21, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023874
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.