510(k) K895759 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
HOLLOW FIBER DIALYZER SERIES FOCUS 160/160H
| Applicant | National Medical Care, Medical Products Div., Inc., Rockleigh NJ, US |
| Decision | Substantially Equivalent, Nov 8, 1989 |
| Received | Sep 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895759
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.