510(k) K970739 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
RMI HEMOCONCENTRATOR PREFERENCE PACK
| Applicant | Research Medical, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Jul 8, 1997 |
| Received | Feb 28, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970739
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.