Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K200524 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| syngo.via RT Image Suite upgraded to VB60 running on SOMATOM go.Sim Model Number 11061660. Running... | 2 | 04/22/2022 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| syngo.via RT Image Suite upgraded to VB60 running on SOMATOM go.Open Pro Model Number 11061670. R... | 2 | 04/22/2022 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Computed tomography x-ray systems with software syngo.CT VA20A_SP4a, VA20A_SP5, VA30A_SP2, VA30A_SP2... | 2 | 09/21/2021 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| syngo.CT VA20A, VA30A and VA40A in: syngo.via RT Image Suite / Sim&Go SOMATOM go.Now SOMATOM ... | 2 | 09/10/2021 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed tomography systems as fo... | 2 | 03/15/2021 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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