510(k) K960474 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
COBE CENTRYSYSTEM 600 HG HEMODIALYZERS
| Applicant | Cobe Renal Care, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Aug 14, 1996 |
| Received | Feb 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960474
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.