510(k) K843014 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FRESENIUS HAEMODIALYSIS A2008
| Applicant | Seratronics, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Oct 18, 1984 |
| Received | Jul 31, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843014
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.