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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K023178
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Product Description
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FDA Recall
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GE Healthcare Innova 4100/ 4100 IQ Digital Fluoroscopic Imaging System (Vascular Angiography System... 2 06/09/2007 General Electric Med Systems LLC
GE Healthcare Innova 4100/4100 IQ. Digital Fluoroscopic Imaging System (Vascular Angiography System... 2 06/05/2007 General Electric Med Systems LLC
GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging System (Versatile cardiac and vascular) 2 06/05/2007 General Electric Med Systems LLC
GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular Imaging Sys... 2 06/05/2007 General Electric Med Systems LLC
GE Healthcare Innova 4100 and Innova 4100 with Bolus Chasing offered as an option. Digital Fluorosc... 2 05/24/2006 GE Healthcare
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