Medical Device Recalls
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1 result found
510(K) Number: K002609 |
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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 Tina-quant RF II; catalog # 3004902 | 3 | 07/19/2003 |
FEI # 1823260 Roche Diagnostics Corp. |
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