510(k) K850866 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1L
| Applicant | Erika, Inc., Rockleigh NJ, US |
| Decision | Substantially Equivalent, Apr 3, 1985 |
| Received | Mar 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850866
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.