Medical Device Recalls
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1 result found
510(K) Number: K151159 |
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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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Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for st... | 2 | 04/22/2016 | Elekta, Inc. |
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