Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K980169 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GE Healthcare CT/e and HiSpeed X/i, families of computed tomography Systems with Gantry. The CT/e... | 2 | 09/18/2009 | GE Medical Systems, LLC |
| Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite;... | 2 | 02/24/2005 | General Electric Med Systems LLC |
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