Medical Device Recalls
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1 result found
510(K) Number: K911959 |
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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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3) Signa Advantage (K911959 Signa Advantage MR System) A magnetic resonance diagnostic device... | 2 | 02/24/2011 | GE Healthcare, LLC |
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