510(k) K870725 ยท FJI Dialyzer, Capillary, Hollow Fiber
FRESENIUS HEMOFLOW F6 AND F8
| Applicant | Seratronics, Inc., Concord CA, US |
| Decision | Substantially Equivalent, May 1, 1987 |
| Received | Feb 24, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870725
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.