510(k) K890315 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
CAPILLARY FLOW DIALYZERS MODELS CT110G & CT190G
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Feb 8, 1989 |
| Received | Jan 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890315
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.