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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K081091
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Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnos... 2 06/10/2019 FEI # 2126677
GE Healthcare, LLC
Precision 500D 2 12/23/2016 FEI # 2126677
GE Healthcare, LLC
GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems. The Precision ... 2 02/03/2014 FEI # 2126677
GE Healthcare, LLC
GE Healthcare Precision 500D, Classical R&F System. Product Usage: The Precision 500D R&F X-... 2 10/02/2014 FEI # 2126677
GE Healthcare, LLC
GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems. A... 2 07/02/2015 FEI # 2126677
GE Healthcare
GE Healthcare Precision 500D Classical R & F system. 2 07/20/2015 FEI # 2126677
GE Healthcare
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