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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K063153
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Product Description
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Recall
Class
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FDA Recall
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NovaPACS  versions 7.4, 7.5, 7.6, and 8.0, Diagnostic Viewer. Distributed by Novarad Corporation. P... 2 07/11/2016 FEI # 1000117423
Novarad Corporation
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