Dia Imaging Analysis, Ltd.
FDA 510(k) & PMA Approved Devices — 10 products
Total Devices10
Categories1
Latest Approval2025-03-17
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K243862 | LVivo Software Application | QIH | 2025-03-17 | View |
| 510(k) | K243331 | LVivo Seamless | QIH | 2025-03-06 | View |
| 510(k) | K243235 | LVivo Software Application | QIH | 2025-03-03 | View |
| 510(k) | K240553 | LVivo Software Application | QIH | 2024-10-04 | View |
| 510(k) | K240769 | LVivo IQS | QIH | 2024-05-24 | View |
| 510(k) | K222970 | LVivo IQS | QIH | 2023-02-01 | View |
| 510(k) | K212466 | LVivo Seamless | QIH | 2021-12-09 | View |
| 510(k) | K210053 | LVivo Software Application | QIH | 2021-02-05 | View |
| 510(k) | K202546 | LVivo Seamless | QIH | 2020-09-29 | View |
| 510(k) | K200232 | LVivo Software Application | QIH | 2020-06-23 | View |
No matching devices.