510(k) K231748
K231748 is an FDA 510(k) premarket notification submitted by Canon Medical Systems Corporation for the device "Cartesion Prime (PCD-1000A/3) V10.15". The FDA issued a decision of Substantially Equivalent on September 12, 2023. The device falls under product code KPS (System, Tomography, Computed, Emission), a Class II device regulated under 21 CFR 892.1200. Canon Medical Systems Corporation has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 12, 2023
- Date Received
- June 15, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Tomography, Computed, Emission
- Device Class
- Class II
- Regulation Number
- 892.1200
- Review Panel
- RA
- Submission Type