Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K193326 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Artis icono floor-angiography systems developed for single and biplane diagnostic imaging and interv... | 2 | 06/07/2022 | Siemens Medical Solutions USA, Inc |
Artis Icono, Interventional Fluoroscopic X-Ray System, Model No. 11327600 | 2 | 07/06/2022 | Siemens Medical Solutions USA, Inc |
syngo Application software VE20 (Material Number 10848815) installed on the Artis pheno and Artis i... | 2 | 07/06/2022 | Siemens Medical Solutions USA, Inc |
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