Medical Device Recalls
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1 result found
510(K) Number: K030534 |
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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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VariSeed 7.1, software application, part number H62, manufactured by Varian Medical Systems. VariSee... | 2 | 04/10/2012 | Varian Medical Systems, Inc. |
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