Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K192061 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now 11061610 & 11061618 SO... | 2 | 04/20/2022 | 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 | Siemens Medical Solutions USA, Inc |
-