Imbio, LLC
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K203256 | Imbio RV/LV Software | QIH | 2021-03-09 | View |
| 510(k) | K180129 | Imbio Segmentation Editing Tool software | LLZ | 2018-03-16 | View |
No matching devices.
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