Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K221516 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imagi... | 2 | 07/02/2024 |
FEI # 3004977335 Siemens AG/Siemens Healthcare GmbH |
| ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100 | 2 | 12/09/2023 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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