Agfa N.V.
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| DR 800. Digital Radiography X-ray System. recall (Z-2738-2024) | Agfa N.V. | 2024-08-27 |
| Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, con recall (Z-1462-2024) | Agfa N.V. | 2024-04-02 |
| DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray recall (Z-3245-2018) | Agfa N.V. | 2018-09-25 |
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Every clearance here is in the API, with alerts when new ones post.