Medical Device Recalls
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1 result found
510(K) Number: K031759 |
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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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| Bio-Rad-TOX/See Drug Screen Test (25 tests/box), Catalog number 194-5230; Product is distributed by ... | 2 | 04/10/2007 |
FEI # 2915274 Bio-Rad Laboratories Inc |
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