Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K001341 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Kodak DirectView DR 7100 System, Catalog #133-6049, a digital radiology system. The major system co... | 2 | 07/20/2004 |
FEI # 1315356 Eastman Kodak Co |
| KODAK DirectView DR 7100 System, Catalog # 133-6049. This is a digital radiology system. The major... | 2 | 12/08/2005 |
FEI # 1315356 Eastman Kodak Co |
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