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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K140862
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Product Description
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Recall
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FDA Recall
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Uterine Electromyographic Monitor - Monica Novii Wireless Patch System Product Usage: The Novii ... 2 03/14/2018 GE Healthcare, LLC
Monica Novii Wireless Patch System product Usage: Novii Interface - The Novii Interface is an ac... 2 05/25/2017 MONICA HEALTHCARE LTD
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