Medical Device Recalls
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1 result found
510(K) Number: K032232 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Hitachi AIRIS Elite Magnetic Resonance Imaging Device | 2 | 06/14/2005 |
FEI # 1528028 Hitachi Medical Systems America Inc |
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