510(k) K260456
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 1, 2026
- Date Received
- February 11, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Perfusion, Kidney
- Device Class
- Class II
- Regulation Number
- 876.5880
- Review Panel
- GU
- Submission Type