Dia Imaging Analysis, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K243862 | LVivo Software Application | March 17, 2025 |
| K243331 | LVivo Seamless | March 6, 2025 |
| K243235 | LVivo Software Application | March 3, 2025 |
| K240553 | LVivo Software Application | October 4, 2024 |
| K240769 | LVivo IQS | May 24, 2024 |
| K222970 | LVivo IQS | February 1, 2023 |
| K212466 | LVivo Seamless | December 9, 2021 |
| K210053 | LVivo Software Application | February 5, 2021 |
| K202546 | LVivo Seamless | September 29, 2020 |
| K200232 | LVivo Software Application | June 23, 2020 |