Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K072237 |
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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 Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System... | 2 | 09/26/2012 | Siemens Medical Solutions USA, Inc |
Siemens MAGNETOM Verio Use: Nuclear resonance imaging system | 2 | 04/02/2012 | Siemens Medical Solutions USA, Inc |
MAGNETOM Verio Nuclear magnetic resonance imaging | 2 | 02/23/2011 | Siemens Medical Solutions USA, Inc |
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