DynamicIQ
FDA 510(k) K222895 · GE Medical Systems SCS
510(k) numberK222895
Submission
- Device name
- DynamicIQ
- Applicant
- GE Medical Systems SCS
Buc, FR - Received
- September 23, 2022
- Decision date
- November 22, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code KPS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261305 | Micsi-PetKPS · Traditional | Microstructure Imaging, Inc. | 09/11/2026SE |
| K261427 | uMI Panvivo (uMI Panvivo M)KPS · Traditional | Shanghai United Imaging Healthcare Co., Ltd. | 07/28/2026SE |
| K261315 | Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7…KPS · Special | Siemens Medical Solutions USA, Inc. | 05/21/2026SE |
| K260524 | uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S)…KPS · Traditional | Shanghai United Imaging Healthcare Co., Ltd. | 04/03/2026SE |
| K253564 | uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX)…KPS · Traditional | Shanghai United Imaging Healthcare Co., Ltd. | 02/13/2026SE |
| K254001 | VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400…KPS · Special | Spectrum Dynamics Medical, Ltd. | 01/13/2026SE |
| K253844 | AnyScan 3.0 NM Scanner FamilyKPS · Traditional | Mediso Medical Imaging Systems, Ltd. | 12/30/2025SE |
| K251370 | Cartesion Prime (PCD-1000A/3) V10.21KPS · Traditional | Canon Medical Systems Corporation | 12/01/2025SE |
| K251401 | PennPET Explorer Positron Emission TomographKPS · Traditional | Trustees of the University of Pennsylvania | 11/25/2025SE |
| K252477 | Hybrid Viewer (00859873006240)KPS · Special | Hermes Medical Solutions AB | 09/09/2025SE |
More from Hermes Medical Solutions AB
| 510(k) | Device | Decision |
|---|---|---|
| K253770 | CardIQ SuiteJAK · Traditional | 07/21/2026SE |
| K260087 | Senographe Pristina; SenoBright HD; Pristina Serena; Pristina Serena BrightMUE · Traditional | 03/24/2026SE |
| K251199 | Allia MoveoOWB · Traditional | 12/09/2025SE |
| K243672 | CardIQ SuiteJAK · Traditional | 06/18/2025SE |
| K243651 | VersaViewerLLZ · Traditional | 04/21/2025SE |
| K243446 | 3DXROWB · Traditional | 02/25/2025SE |
| K233731 | CardIQ SuiteJAK · Traditional | 08/01/2024SE |
| K233714 | BreViewLLZ · Traditional | 01/25/2024SE |
| K232344 | Allia IGS 3, Allia IGS 5, Allia IGS 7, Allia IGS 7 OROWB · Special | 10/11/2023SE |
| K223424 | Spine Auto ViewsJAK · Traditional | 07/13/2023SE |
Questions and answers
When was DynamicIQ cleared by the FDA?
DynamicIQ (K222895) received a 510(k) decision of Substantially Equivalent on November 22, 2022, 60 days after the submission was received.
What is the product code of K222895?
The FDA product code is KPS – System, Tomography, Computed, Emission, a Class II (moderate risk) device regulated under 21 CFR 892.1200.