Medical Device Recalls
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1 result found
510(K) Number: K171681 |
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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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| Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Hybrid Recon software versions af... | 2 | 12/12/2024 |
FEI # 3002831423 Hermes Medical Solutions AB |
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