Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K022390 |
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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 Altaire Magnetic Resonance Imaging System | 2 | 06/10/2006 | Hitachi Medical Systems America Inc |
| Magnetic Resonance Imaging Device | 2 | 05/31/2006 | Hitachi Medical Systems America Inc |
| Hitachi Altaire Magnetic Resonance Imaging Device. | 2 | 06/14/2005 | Hitachi Medical Systems America Inc |
| Altaire, Magnetic Resonance Imaging Device. | 2 | 05/17/2005 | Hitachi Medical Systems America Inc |
| Altaire, Magnetic Resonance Imaging Device. | 2 | 05/03/2005 | Hitachi Medical Systems America Inc |
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