510(k) K992573 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
AF-220 HEMODIALYZER
| Applicant | Althin Medical AB, Ronneby, SE |
| Decision | Substantially Equivalent, Jan 18, 2000 |
| Received | Aug 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992573
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.