InVision Medical Technology Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K243866 | InVision Precision Cardiac Amyloid | May 21, 2025 |
| K232331 | InVision Precision LVEF (LVEF) | April 25, 2024 |