Medical Device Recalls
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1 result found
510(K) Number: K983439 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (... | 2 | 12/03/2014 |
FEI # 3005094123 Abbott Ireland Diagnostics Division |
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