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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: K033238
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FDA Recall
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Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Mobilett XP and Mobilett XP ... 2 07/02/2014 Siemens Medical Solutions USA, Inc
Mobilett XP Hybrid/Digital/CR Intended use: mobile x-ray system 2 12/17/2010 Siemens Medical Solutions USA, Inc
Mobilett XP and Mobilett XP Hybrid, Mobile radiology device System, x-ray, mobile 2 11/01/2010 Siemens Medical Solutions USA, Inc
Mobilett XP, mobile X-ray system, Model number 1818454 2 04/19/2007 Siemens Medical Solutions USA, Inc
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