Medical Device Recalls
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1 result found
510(K) Number: K103093 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Laksell GammaPlan, a computer based dose planning system specifically designed for use with Leksell ... | 2 | 06/05/2015 | Elekta, Inc. |
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