| Device Type ID | 2008 |
| Device Name | Hemodialyzer, Re-use, High Flux |
| Regulation Description | High Permeability Hemodialysis System. |
| Regulation Medical Specialty | Gastroenterology/Urology |
| Review Panel | Gastroenterology/Urology |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Reproductive, Gastro-Renal, And Urological Devices (DRGUD) Renal Devices Branch (RNDB) |
| Submission Type | 510(k) |
| CFR Regulation Number | 876.5860 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | MSF |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | Yes |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 2008 |
| Device | Hemodialyzer, Re-use, High Flux |
| Product Code | MSF |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | High Permeability Hemodialysis System. |
| CFR Regulation Number | 876.5860 [🔎] |