Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K911667 |
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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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MRP-7000 and AIRIS Magnetic Resonance Imaging Systems, Software Versions: V7.0A to V7.0J. | 2 | 10/12/2006 | Hitachi Medical Systems America Inc |
MRP-7000, AIRIS Magnetic Resonance Imaging Systems | 2 | 06/10/2006 | Hitachi Medical Systems America Inc |
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