Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K211379 |
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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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syngo.via RT Image Suite with syngo.via VB30, VB40, VB50 and VB60- Intended for Radiation Therapy ... | 2 | 09/10/2021 | Siemens Medical Solutions USA, Inc |
syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on s... | 2 | 04/22/2022 | Siemens Medical Solutions USA, Inc |
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