510(k) K003023 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
COBE HC 700 MIDI HEMOCONCENTRATOR
| Applicant | Hospal Industrie, Arvada CO, US |
| Decision | Substantially Equivalent, Apr 30, 2001 |
| Received | Sep 28, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003023
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.