The following data is part of a premarket notification filed by Seratronics, Inc. with the FDA for Fresenius Hemoflow F60 And F80.
| Device ID | K870724 |
| 510k Number | K870724 |
| Device Name: | FRESENIUS HEMOFLOW F60 AND F80 |
| Classification | Dialyzer, High Permeability With Or Without Sealed Dialysate System |
| Applicant | SERATRONICS, INC. 4090 PIKE LN. Concord, CA 94520 |
| Contact | Thomas E Cane |
| Correspondent | Thomas E Cane SERATRONICS, INC. 4090 PIKE LN. Concord, CA 94520 |
| Product Code | KDI |
| CFR Regulation Number | 876.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-02-24 |
| Decision Date | 1987-04-01 |