510(k) K926568 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
BAXTER CT DIALYZER
| Applicant | Baxter Healthcare Corp, Waukegan IL, US |
| Decision | Substantially Equivalent, Sep 30, 1994 |
| Received | Dec 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926568
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.