510(k) K062090 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
PRISMA SYSTEM R03.10A
| Applicant | Gambro Renal Products, Lakewood CO, US |
| Decision | Substantially Equivalent, Oct 18, 2006 |
| Received | Jul 24, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062090
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.