Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K123529 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray | 2 | 03/27/2014 | Siemens Medical Solutions USA, Inc |
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