Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K024200 |
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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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| GE, Innova® 2000 The principle system components include a C-arm, image acquisition, processing and ... | 2 | 09/24/2009 |
FEI # 2126677 GE Medical Systems, LLC |
| Innova 2000's principle system components include a C-arm, image acquisition, processing and archivi... | 2 | 09/16/2008 |
FEI # 2126677 GE Healthcare |
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