Arineta , Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories1
Latest Approval2025-04-15
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K250650 | SpotLight / SpotLight Duo with Low Dose Lung Cancer Screening Option | JAK | 2025-04-15 | View |
| 510(k) | K241200 | SpotLight/SpotLight Duo with Low Dose Lung Cancer Screening Option | JAK | 2025-01-13 | View |
| 510(k) | K230370 | SpotLight/SpotLight Duo (with DLIR option) | JAK | 2023-10-13 | View |
| 510(k) | K213465 | CardioGraphe | JAK | 2022-12-02 | View |
| 510(k) | K161066 | SpotLight CT | JAK | 2016-08-10 | View |
No matching devices.