Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K933018 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Magnetic Resonance Imaging System Core Software, Software installed in all of the following: ... | 3 | 07/20/2004 | Toshiba American Med Sys Inc |
| Magnetic Resonance Imaging, System: Flexart, Visart and Excelart Models. | 3 | 07/20/2004 | Toshiba American Med Sys Inc |
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