Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K181550 |
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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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| Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Model: 11105200 Cios Spin (VA30) - Model:... | 2 | 08/22/2020 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194 | 2 | 05/04/2020 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Cios Spin, Image-Intensified Fluoroscopic X-Ray System The Cios Alpha and Cios Spin are a mobile ... | 2 | 08/26/2020 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Siemens Cios Spin VA30-mobile X-Ray system, Material # 10308194 - Product Usage: The Cios Alpha and... | 2 | 05/04/2020 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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