The following data is part of a premarket notification filed by Amicon, Inc. with the FDA for Hemofilters.
| Device ID | K813591 |
| 510k Number | K813591 |
| Device Name: | HEMOFILTERS |
| Classification | Dialyzer, High Permeability With Or Without Sealed Dialysate System |
| Applicant | AMICON, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KDI |
| CFR Regulation Number | 876.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-28 |
| Decision Date | 1982-03-31 |