510(k) K982926 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FRESENIUS BLOOD VOLUME MONITOR
| Applicant | Fresenius Medical Care North America, Wrentham MA, US |
| Decision | Substantially Equivalent, Sep 3, 1999 |
| Received | Aug 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982926
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.