Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K002531 |
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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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| 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 Systems; Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN ... | 2 | 07/13/2005 | Toshiba American Med Sys Inc |
| Magnetic Resonance Imaging Systems under the following names: Visart Excelart Excelart P2 Exce... | 2 | 12/02/2004 | Toshiba American Med Sys Inc |
| Magnetic Resonance Imaging System(s) Visart and Exelart P2/ Exelart P3/ Exelart SPIN and Exelart ... | 2 | 07/20/2004 | Toshiba American Med Sys Inc |
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