510(k) K962427 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
COBE CENTRYSYSTEM 700 HG HEMODIALYZER
| Applicant | Gambro Healthcare, Lakewood CO, US |
| Decision | Substantially Equivalent, Sep 20, 1996 |
| Received | Jun 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962427
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.