510(k) K844663 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ASAHI NEW PAN-SERIES HEMOFILTERS
| Applicant | Asahi Medical Co., Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Jan 18, 1985 |
| Received | Nov 30, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844663
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.