510(k) K013733 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
SYSTEM 100; S-100 ULTRAFILTRATION CONSOLE; BDT 500 ULTRAFILTRATION SET
| Applicant | Chf Solutions, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 3, 2002 |
| Received | Nov 9, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013733
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.