Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K220432 |
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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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| ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imagi... | 2 | 07/02/2024 | Siemens AG/Siemens Healthcare GmbH |
| ARTIS icono biplane -Angiography systems developed for single and biplane diagnostic imaging and int... | 2 | 08/08/2023 | Siemens Medical Solutions USA, Inc |
| ARTIS icono floor-Angiography systems developed for single and biplane diagnostic imaging and interv... | 2 | 08/08/2023 | Siemens Medical Solutions USA, Inc |
| Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700 | 2 | 08/26/2022 | Siemens Medical Solutions USA, Inc |
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