510(k) K243840
K243840 is an FDA 510(k) premarket notification submitted by Bridge TO Life for the device "Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)". The FDA issued a decision of Substantially Equivalent on March 26, 2025. The device falls under product code KDN (System, Perfusion, Kidney), a Class II device regulated under 21 CFR 876.5880. Bridge TO Life has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 26, 2025
- Date Received
- December 13, 2024
- 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