Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K180589 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DR 800. Digital Radiography X-ray System. | 2 | 08/27/2024 |
FEI # 3001556265 Agfa N.V. |
| AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product U... | 2 | 06/03/2020 |
FEI # 3001556265 Agfa N.V. |
| AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 8... | 2 | 07/30/2019 |
FEI # 3001556265 Agfa N.V. |
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