Medical Device Recalls
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1 to 10 of 29 Results
510(K) Number: K052202 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Artis systems - Product Usage: an angiography systems developed for single and biplane diagnostic im... | 2 | 04/26/2021 | Siemens Medical Solutions USA, Inc |
AXIOM Artis MP, Model Number 5904466 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis dBC, Model Number 7728392 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis TC, Model Number 7728350 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis dFC, Model Number 7727717 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis dFA, Model Number 7555373 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis dMP, Model Number 7555365 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis dBA, Model Number 7555357 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis dTC, Model Number 7413078 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
AXIOM Artis dFC, Model Number 7412807 | 2 | 07/22/2019 | Siemens Medical Solutions USA, Inc |
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