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U.S. Department of Health and Human Services

Medical Device Recalls

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Date Classified to: 10/23/2014 510(K) Number: K123197
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Product Description
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Recall
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The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative, multiplexed in vitro di... 2 Sep-23-2014 Nanosphere, Inc.
Nanosphere Verigene Each CDF test consists of a Verigene CDF Nucleic Acid Test Kit and a Verigen... 3 Aug-08-2014 Nanosphere, Inc.
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