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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: K011135
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Product Description
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Recall
Class
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FDA Recall
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GSI Audera (version 2.6 software) Viasys Healthcare, Inc. Part or (Catalog) Numbers: 2001-9700, 2... 2 11/12/2008 Cardinal Health, Inc
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