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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K122286
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FDA Recall
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MAMMOMAT Inspiration. Intended for mammography exams, screening, diagnosis, and stereotactic biop... 2 05/20/2014 Siemens Medical Solutions USA, Inc
Mammomat Inspiration full, field digital,system,x-ray,mammographic Product Usage: The Mammomat I... 2 01/31/2017 Siemens Medical Solutions USA, Inc
Mammomat Inspiration system: Product Usage: mammography exams, screening, diagnosis, and stereo... 2 12/06/2014 Siemens Medical Solutions USA, Inc
Siemens Mammomat Inspiration - full-field digital mammography Product Usage: Mammography 2 07/11/2013 Siemens Medical Solutions USA, Inc
Siemens Mammomat Inspiration mammography systems. The Mammomat Inspiration system is intended fo... 2 10/17/2014 Siemens Medical Solutions USA, Inc
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