Medical Device Recalls
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1 result found
510(K) Number: K101751 |
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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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Varian Unique Single Energy Linear Accelerator, C-Series Clinac or Trilogy, versions 7.x and 8.x, Re... | 2 | 01/11/2012 | Varian Medical Systems, Inc. Oncology Systems |
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