Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K250660 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 1157400... | 2 | 01/27/2026 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 1157400... | 2 | 01/27/2026 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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