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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K032370
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Product Description
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FDA Recall
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CIC Pro Clinical Information Center Central Station - Product Usage: The intended use is to provide ... 2 12/20/2019 GE Healthcare, LLC
GE Healthcare CIC Pro" Software Versions 5.0.3, 5.0.6 ,5.0.7, 5.0.8 and 4.1. The CIC Pro" Clinic... 2 05/04/2009 GE Medical Systems Information Tecnology
GE Healthcare CIC Pro Clinical Information Center, Central Station, Software Version 4.1. (CIC Pro v... 2 02/01/2008 General Electric Medical Systems Information Technology
GE Healthcare CIC Pro Clinical Information Center, Central Station, Software Version 4.1. , GE Medic... 2 06/06/2007 General Electric Medical Systems Information Technology
GE CIC Central Station Monitoring Product, Versions 3.x, 4.0.5, 4.0.6 2 10/21/2004 General Electric Medical Systems Information Technology
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