Medical Device Recalls
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1 result found
510(K) Number: K212604 |
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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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| The following Pro.specta Emission Computed Tomography Systems that were manufactured with an SLD Loo... | 2 | 07/28/2023 |
FEI # 1000514697 Siemens Medical Solutions USA, Inc. |
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