Medical Device Recalls
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1 result found
510(K) Number: K926442 |
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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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Premier brand C. difficile Toxin A, diagnstic test kits, one kit per pouch, one pouch per shipping b... | 2 | 01/23/2003 | Meridian Bioscience Inc |
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