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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 19 of 19 Results
510(K) Number: K052293
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Product Description
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GE Healthcare, SIGNA HDxt 3.0T. Product Usage: The 1.5T Signa HDx family and 3.0T Signa HDx fami... 2 11/10/2015 GE Healthcare
SIGNA INFINITY MR SYSTEM WITH EXCITE TECHNOLOGY GE 3.0T SIGNA INFINITY TWINSPEED WITH EXCITE MR SY... 2 08/09/2013 GE Healthcare, LLC
GE Healthcare, Discovery MR750, Discovery 450, Optima 450W (with and without GEM), Signa HDx, Signa ... 2 05/01/2013 GE Healthcare, LLC
Optima MR450w, Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, Signa Vibrant, an... 2 03/11/2013 GE Healthcare, LLC
5) Signa HDx (K052293 Signa HDx and HDxt MR Systems) Signa HDx or Signa HDxt (K052293 Signa ... 2 02/24/2011 GE Healthcare, LLC
Signa Excite 1.5T, Signa HD 1.5T, Signa HDx 1.5T, Signa HDxT 1.5T, Signa HDe, GE DISCOVERY MR450 and... 2 01/11/2010 GE Medical Systems, LLC
GE 1.5T and 3.0T Signa HDx MR System The product is used as a diagnostic imaging device to produce... 2 09/17/2008 GE Healthcare
GE 1.5T and 3.0T Signa® HDx MR System Model Numbers: 5127452, 2377062-61, and 2395001-2. Indica... 2 09/16/2008 GE Healthcare
GE 1.5T and 3.0T Signa HDX MR System Model Number(s): 2226300, 2377062-61, 2395001, 2395001-2, 510... 2 09/11/2008 GE Healthcare
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