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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K880530
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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VersaRad/Traumex General Radiographic System. 2 07/20/2004 Fischer Imaging Corporation
VersaRad Generator 2 05/03/2005 Fischer Imaging Corporation
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