Medical Device Recalls
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1 result found
510(K) Number: K152393 |
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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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Eclipse Treatment Planning System versions 11, 13.0, 13.5 and 13.6; Model number: H48; Product U... | 2 | 02/12/2016 | Varian Medical Systems, Inc. |
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