Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K901003 |
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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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| Roche/Hitachi 747 - 200 clinical chemistry analyzer; catalog number 04009223680. | 2 | 09/02/2004 |
FEI # 1823260 Roche Diagnostics Corp. |
| Roche/Hitachi 747 - 100 clinical chemistry analyzer; catalog number 04009223680. | 2 | 09/02/2004 |
FEI # 1823260 Roche Diagnostics Corp. |
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