Medical Device Recalls
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1 result found
510(K) Number: K121434 |
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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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MAGNETOM systems Aera/Skyra/Avanto/Verio with software syngo MR D13A ; indicated for use as magneti... | 2 | 03/20/2015 | Siemens Medical Solutions USA, Inc |
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