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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Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS icono floor- 11327700... | 2 | 04/26/2021 | Siemens Medical Solutions USA, Inc |
Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnosti... | 2 | 03/22/2021 | 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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