Medical Device Recalls
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1 result found
510(K) Number: K900940 |
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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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| Package Insert for TDx/TDxFLx and TDxFLx Phenobarbital II Reagents, REF 9500, item number 69-5162/R4... | 2 | 07/20/2004 | Abbott Laboratories HPD/ADD/GPRD |
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