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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
Product: ivi Recall Date to: 07/05/2014
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iView DAB Detection Kit, Part number: 760-091 (05266157001) This detection kit is intended for i... 2 07/01/2011 FEI # 1000125183
Ventana Medical Systems Inc
iVIEW DAB Detecion Kit. Catalog Number 760-091 3 06/17/2003 FEI # 1000125183
Ventana Medical Systems Inc
iView GT Electronic Portal Imaging Device, used with radiation therapy treatments. 2 04/26/2010 FEI # 1037831
Elekta, Inc.
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