Medical Device Recalls
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1 result found
510(K) Number: K833070 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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IMx Theophylline Reagent Pack (List 1A81-20) In Vitro test. This reagent system is composed of one ... | 2 | 07/03/2007 | Abbott Diagnostic International, Ltd. |
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