Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K192065 |
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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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Software: Syngo.via RT Image Suite software version VA30_SP02 with license T_RT_IMAGE_SUITE_PAT_MARK... | 2 | 09/23/2020 | Siemens Medical Solutions USA, Inc |
syngo.via RT Image Suite with software versions syngo.via VB30 or VB40 | 2 | 07/22/2020 | Siemens Medical Solutions USA, Inc |
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