FDA 510(k) Applications Submitted by Imbio, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180129 | 01/17/2018 | Imbio Segmentation Editing Tool software | Imbio, LLC |
| K203256 | 11/04/2020 | Imbio RV/LV Software | Imbio, LLC |
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