510(k) K070049
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 3, 2011
- Date Received
- January 4, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Hemodialysis System For Home Use
- Device Class
- Class II
- Regulation Number
- 876.5860
- Review Panel
- GU
- Submission Type
To treat and provide hemodialysis therapy at home for chronic renal failure patients.