510(k) K850655 ยท FJI Dialyzer, Capillary, Hollow Fiber
TORAY IND. FILTRYZER HOLLOW FIBER ARTIF. KIDNEY B2
| Applicant | Erika, Inc., Rockleigh NJ, US |
| Decision | Substantially Equivalent, Mar 7, 1985 |
| Received | Feb 19, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850655
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.