| Device |
system, dialysate delivery, central multiple patient |
| Regulation Description |
Hemodialysis system and accessories. |
| Regulation Medical Specialty |
Gastroenterology/Urology |
| Review Panel |
Gastroenterology/Urology |
| Product Code | FKQ |
| Submission Type |
510(k)
|
| Regulation Number |
876.5820
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
| Recognized Consensus Standards
|
Guidance Documents
- Regulatory Status of Disinfectants Used to Process Dialysate Delivery Systems and Water Purification Systems for Hemodialysis; Guidance for Industry and FDA
- Guidance on the Content of Premarket Notification [510(k)] Submissions for Protective Restraints
|
|
| Third Party Review |
Not Third Party Eligible |