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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: K924452
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Product Description
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Recall
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FDA Recall
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Edwards Lifesciences Swan-Ganz CCOombo CCO/SvO2 Thermodilution Catheter with AMC THROMBOSHIELD (an ... 2 04/17/2009 Edwards Lifesciences, Llc
EDWARDS VIGILANCE MONITORS (FORMERLY BAXTER VIGILANCE MONITORS) with software release 5.3 or earli... 2 08/02/2006 Edwards Lifesciences Llc
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