Medical Device Recalls
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1 result found
510(K) Number: K936229 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| TOSOH ST AIA- PACK TT3, Lot FX17440, catalog #025282. This reagent is used for the quantitat... | 3 | 02/23/2006 | Tosoh Bioscience Inc |
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