Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K183034 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MOSAIQ Oncology Information System | 2 | 09/29/2021 | Elekta, Inc. |
| Elekta MOSAIC Oncology Information System versions: 2.62, 2.64, 2.70, 2.81, 2.82, and 2.83 hosted o... | 2 | 06/02/2021 | Elekta, Inc. |
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