510(k) K883748 ยท FJI Dialyzer, Capillary, Hollow Fiber
RENAK-E & RENEK-A SERIES HOLLOW FIBER DIALYZERS
| Applicant | Kawasumi Laboratories Co., Ltd., Tokyo, JP |
| Decision | Substantially Equivalent, Jan 31, 1989 |
| Received | Sep 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883748
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.