510(k) K883307 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
CARDIOFLOW 100 HEMOCONCENTRATOR/PREPARATION KIT
| Applicant | Hospal Medical Corp., Edison NJ, US |
| Decision | Substantially Equivalent, Oct 12, 1988 |
| Received | Aug 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883307
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.