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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K002531
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Product Description
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FDA Recall
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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(s) Visart and Exelart P2/ Exelart P3/ Exelart SPIN and Exelart ... 2 07/20/2004 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 Systems; Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN ... 2 07/13/2005 Toshiba American Med Sys Inc
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