Medical Device Recalls
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1 result found
510(K) Number: K152880 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combine... | 2 | 01/10/2019 | Siemens Medical Solutions USA, Inc. |
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