Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032232 |
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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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Magnetic Resonance Imaging Device | 2 | 05/31/2006 | Hitachi Medical Systems America Inc |
Hitachi AIRIS Elite Magnetic Resonance Imaging Device | 2 | 06/14/2005 | Hitachi Medical Systems America Inc |
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