Argus Cognitive, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K260064 | Neurora | QPF | 2026-10-02 | View |
| 510(k) | K251417 | ReVISION 2 | QIH | 2026-09-09 | View |
| 510(k) | K223322 | Argus Cognitive ReVISION Software | LLZ | 2023-07-24 | View |
No matching devices.
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