Medical Device Recalls
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31 to 35 of 35 Results
510(K) Number: K073290 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Mavig Portegra 2 which is an accessory to the Siemens angiographic, fluoroscopic and radiographic im... | 2 | 06/16/2009 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Siemens Artis zee Ceiling Systems. Angiographic x-ray system. | 2 | 02/24/2014 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnosti... | 2 | 08/05/2015 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| The Artis zee / zeego Angiography System is designed as a set of components that may be combined in... | 2 | 12/01/2014 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| system, x-ray, angiographic, model # 10094135, 10094137, 10094139, 10094141, 10280959 Artis zee/ ... | 2 | 03/31/2016 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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