510(k) K914020 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
MODIFIED ASAHI PAN-SERIES HEMOFILTERS
| Applicant | Asahi Medical Co., Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Mar 20, 1992 |
| Received | Sep 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914020
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.