| Device |
set, tubing, blood, with and without anti-regurgitation valve |
| Regulation Description |
Hemodialysis system and accessories. |
| Regulation Medical Specialty |
Gastroenterology/Urology |
| Review Panel |
Gastroenterology/Urology |
| Product Code | FJK |
| 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 Standard
|
Guidance Document
- Guidance for Industry and FDA Staff: Hemodialysis Blood Tubing Sets - Premarket Notification [510(k)] Submissions
|
|
| Third Party Review |
Not Third Party Eligible |
|
|