Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K013608 |
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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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| Toshiba Digital Radiography System Model DFP8000D | 2 | 02/23/2006 |
FEI # 2020563 Toshiba American Med Sys Inc |
| Digital Radiography System, model DFP-8000D | 2 | 08/11/2004 |
FEI # 2020563 Toshiba American Med Sys Inc |
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