510(k) K122241
K122241 is an FDA 510(k) premarket notification submitted by Cardiovascular Imaging Technologies for the device "IMAGEN3D". The FDA issued a decision of Substantially Equivalent on Oct 24, 2012. The device falls under product code KPS (System, Tomography, Computed, Emission), a Class II device regulated under 21 CFR 892.1200. Cardiovascular Imaging Technologies has 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 24, 2012
- Date Received
- Jul 27, 2012
- 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
- 510(k)