Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K150595 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Hitachi Scenaria Whole-body X-ray CT System | 2 | 11/01/2019 |
FEI # 1528028 Hitachi Medical Systems America Inc |
| Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole bo... | 2 | 08/17/2018 |
FEI # 1528028 Hitachi Medical Systems America Inc |
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