Medical Device Recalls
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1 result found
510(K) Number: K102915 |
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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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| ViewRay MRIdian Linac System: Model No. 20000-01 software, CE 0086 - Product Usage: intended to be ... | 2 | 06/09/2021 |
FEI # 3011233554 Viewray, Inc. |
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