Medical Device Recalls
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1 result found
510(K) Number: K102489 |
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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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Titan 3T MRI System, MRT-3010A/5. Product Usage: Usage: MRI system. | 2 | 11/13/2013 | Toshiba American Medical Systems Inc |
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