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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K111582
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FDA Recall
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GE Healthcare, LOGIQ S8 Ultrasound System The device is intended for use by a qualified physicia... 2 08/09/2013 FEI # 2126677
GE Healthcare, LLC
GE Healthcare, LOGIQ S8 DIAGNOSTIC ULTRASOUND SYSTEM with R1.1.0 Software. Intended for use by a... 2 02/23/2012 FEI # 2126677
GE Healthcare, LLC
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