Medical Device Recalls
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1 result found
510(K) Number: K071925 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Siemens MAGNETOM Essenza, Nuclear Magnetic Resonance Imaging System Product Usage: Nuclear mag... | 2 | 05/25/2012 | Siemens Medical Solutions USA, Inc |
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