Medical Device Recalls
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1 result found
510(K) Number: K161146 |
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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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| Upper roller bracket (part number 1088370) for the Gen2 gantry enclosure for the Radixact Treatment ... | 2 | 08/31/2023 |
FEI # 3003873069 Accuray Incorporated |
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