510(k) K920757 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FILTRAL HEMODIALYZERS
| Applicant | C.G.H. Medical, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Aug 5, 1994 |
| Received | Feb 19, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920757
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.