510(k) K883195 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FRESENIUS F8 DIALYZER
| Applicant | Fresenius USA, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Sep 13, 1988 |
| Received | Jul 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883195
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.