510(k) K874872 ยท FJI Dialyzer, Capillary, Hollow Fiber
FRESENIUS HEMOFLOW F3, F4, F5, F7
| Applicant | Seratronics, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Feb 19, 1988 |
| Received | Nov 27, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874872
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 5, 2016 | Fresenius Medical Care Renal Therapies Group, LLC Fresenius Hemoflow F3 Dialyzer
Part Number: 0520165A
Indicated for Acute and Chronic Hemodialysis Terminated |
FJI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.