Medical Device Recalls
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1 result found
510(K) Number: K940534 |
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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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Gyroscan NT MRI System rev 4.x, 5.x, and 6.x software. System, Nuclear Magnetic Resonance imaging. | 2 | 01/06/2006 | Philips Medical Systems North America Co. Phillips |
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