Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K220409 |
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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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ARTIS pheno-Angiography systems developed for single and biplane diagnostic imaging and intervention... | 2 | 08/08/2023 | Siemens Medical Solutions USA, Inc |
Artis pheno- Model No. 10849000 | 2 | 08/26/2022 | Siemens Medical Solutions USA, Inc |
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