510(k) K890111 ยท FJI Dialyzer, Capillary, Hollow Fiber
GAMBRO ALWALL GFE 8 & 9 HOLLOW FIBER DIALYZER
| Applicant | Gambro, Inc., Lincolnshire IL, US |
| Decision | Substantially Equivalent, Feb 8, 1989 |
| Received | Jan 11, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890111
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.