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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K133535
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INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM 2 03/02/2018 Toshiba American Medical Systems Inc
INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems 2 02/09/2016 Toshiba American Medical Systems Inc
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