Medical Device Recalls
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1 result found
510(K) Number: K171837 |
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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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| TomoTherapy Treatment Delivery System with iDMS - Product Usage: used as an integrated system for th... | 2 | 01/07/2021 |
FEI # 3003873069 Accuray Incorporated |
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