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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
510(K) Number: K031571
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Product Description
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Recall
Class
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FDA Recall
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Brand Name: EmpowerCT/EmpowerCTA Injector System Ceiling Column Accessory; Common/Usual Name: CT Inj... 2 02/16/2005 E-Z-EM, Inc
Brand Name of Device: EmpowerCT/EmpowerCTA Injector System Ceiling Column Accessory; Common/Usual Na... 2 02/16/2005 E-Z-EM, Inc
Brand Name: EmpowerCT/EmpowerCTA Injector System Ceiling Column Accessory; Common/Usual Name: CT In... 2 02/16/2005 E-Z-EM, Inc
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