510(k) K120331
K120331 is an FDA 510(k) premarket notification submitted by Siemens AG Medical Solutions for the device "SYNGO CT DYNAMIC ANGIO". The FDA issued a decision of Substantially Equivalent on April 13, 2012. The device falls under product code JAK (System, X-Ray, Tomography, Computed), a Class II device regulated under 21 CFR 892.1750. Siemens AG Medical Solutions has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 13, 2012
- Date Received
- February 2, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, X-Ray, Tomography, Computed
- Device Class
- Class II
- Regulation Number
- 892.1750
- Review Panel
- RA
- Submission Type