Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K123230 |
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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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| MOSAIQ(R) Oncology Information System, Versions 2.50.05 and higher Product Usage: MOSAIQ® is an ... | 2 | 06/27/2017 |
FEI # 1037831 Elekta, Inc. |
| MOSAIQ Oncology Information System | 2 | 07/27/2016 |
FEI # 1037831 Elekta, Inc. |
| MOSAIQ Product Usage: MOSAIQ is an oncology information system used to manage workflows for trea... | 2 | 11/15/2014 |
FEI # 1037831 Elekta, Inc. |
| MOSAIQ MOSAIQ is an oncology information system used to manage workflows for treatment planning a... | 2 | 06/25/2014 |
FEI # 1037831 Elekta, Inc. |
| MOSAIQ, an oncology information system used to manage workflows for treatment planning and delivery.... | 2 | 06/16/2014 |
FEI # 1037831 Elekta, Inc. |
| ELEKTA MOSAIQ SW version below 2.41 Product Usage: The intended use of the SIEMENS branded ARTIS... | 2 | 04/10/2013 |
FEI # 2937457 Siemens Medical Solutions USA, Inc |
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