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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K960575
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Product Description
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FDA Recall
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GE Healthcare, Advantx, Innova 2000, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova ... 2 10/17/2013 FEI # 2126677
GE Healthcare, LLC
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems... 2 02/05/2016 FEI # 2126677
GE Medical Systems, LLC
ADVANTX LCV+ 2 12/23/2016 FEI # 2126677
GE Healthcare, LLC
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