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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 17 of 17 Results
510(K) Number: K031077
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Product Description
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FDA Recall
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INTELECT ADVANCED, Model No. 2772MC, Chattanooga Group, Hixson, TN 37343, Made in the USA, Not for ... 2 06/25/2008 FEI # 1000342033
Chattanooga Corp Inc
INTELECT ADVANCED STIM, Model No. 2773MS, Chattanooga Group, Hixson, TN 37343, Made in the USA, Not... 2 06/25/2008 FEI # 1000342033
Chattanooga Corp Inc
INTELECT MOBILE COMBO, Model No. 2778, Chattanooga Group, Hixson, TN 37343, Made in the USA, Not fo... 2 06/25/2008 FEI # 1000342033
Chattanooga Corp Inc
INTELECT MOBILE, Model No. 2777, Chattanooga Group, Hixson, TN 37343, Made in the USA, Not for sale... 2 06/25/2008 FEI # 1000342033
Chattanooga Corp Inc
VECTRA GENISYS, Model No. 2761, Chattanooga Group, Hixson, TN 37343, Made in the USA 2 06/25/2008 FEI # 1000342033
Chattanooga Corp Inc
INTELECT INTELECT XT, Model No. 2760, Chattanooga Group, Hixson, TN 37343, Made in the USA 2 06/25/2008 FEI # 1000342033
Chattanooga Corp Inc
INTELECT LEGEND XT, Model No. 2763, Chattanooga Group, Hixson, TN 37343, Made in the USA 2 06/25/2008 FEI # 1000342033
Chattanooga Corp Inc
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