Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K170434 |
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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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| Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of mu... | 2 | 10/10/2024 |
FEI # 3009471886 Agfa Healthcare NV |
| Agfa HealthCare Enterprise Imaging XERO Viewer | 2 | 01/20/2023 |
FEI # 3009471886 Agfa Healthcare NV |
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