Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K183275 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Produ... | 2 | 03/18/2020 | Agfa N.V. |
| Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common Name: DR 800 ... | 2 | 12/22/2025 | AGFA Healthcare Corp. |
| DR 800. Digital Radiography X-ray System. | 2 | 08/27/2024 | Agfa N.V. |
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