FDA 510(k) Applications Submitted by InVision Medical Technology Corporation
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K232331 | 08/04/2023 | InVision Precision LVEF (LVEF) | InVision Medical Technology Corporation |
| K243866 | 12/17/2024 | InVision Precision Cardiac Amyloid | InVision Medical Technology Corporation |
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