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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 34 Results
510(K) Number: K042053
 
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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 3100/ 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular Imaging Syst... 2 07/10/2007 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 Advantx, Innova2000, Innova3100, Innova4100, Innova2100IQ, Innova3100IQ, and Innova41... 2 03/13/2013 GE Healthcare, LLC
GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging System (Versatile cardiac and vascular). 2 07/10/2007 General Electric Med Systems LLC
GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innov... 2 05/14/2013 GE Healthcare, LLC
GE Healthcare Innova 3100 Digital Fluoroscopic Imaging (Cardiovascular Imaging System) 2 09/30/2008 Datex - Ohmeda, Inc
GE Healthcare Innova 3100 Digital Fluoroscopic Imaging System with Bolus Chasing option. 2 09/29/2008 GE Healthcare
GE Healthcare Innova 4100 Digital Fluoroscopic Imaging System with Bolus Chasing option. 2 09/29/2008 GE Healthcare
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