| K-number | K870725 |
| Device name | FRESENIUS HEMOFLOW F6 AND F8 |
| Applicant | Seratronics, Inc. |
| Product code | FJI |
| Device class | Class II |
| Decision date | May 1, 1987 |
| Decision | Substantially Equivalent |
| Regulation | 876.5820 |
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