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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K062154
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Product Description
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FDA Recall
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VitreaCore® software. Versions subject to the limitation: 6.0, 6.1, 6.2, 6.3 (except 6.3.1 ), 6.4 (... 2 11/06/2013 Vital Images, Inc.
Vitrea Enterprise Suite, Vitrea, VitreaAdvanced, VitreaCore (VitalConnect) and Vitrea fX prior to ve... 2 03/27/2013 Vital Images, Inc.
Vital Connect 4.0 & 4.1, radiological image processing software A Medical diagnostic software sys... 2 02/02/2011 Vital Images, Inc.
Vital Images ViTALConnect , Version 4.0 and 4.1, PET/CT Visualization option. Vital Images, Inc., 5... 2 01/31/2008 Vital Images, Inc.
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