Medical Device Recalls
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1 result found
510(K) Number: K883540 |
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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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| Oxoid Infectious Mononucleosis Test, Catalog #DR0680M. The firm name on the label is Oxoid, Ltd., B... | 3 | 04/22/2006 | Remel, Inc. |
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