Medical Device Recalls
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1 result found
510(K) Number: K133572 |
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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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ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1 | 2 | 04/14/2022 | Varian Medical Systems Imaging Laboratory GmbH |
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