Medical Device Recalls
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1 result found
510(K) Number: K843347 |
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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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| Anti-dsDNA [125I] Radiobinding Assay Kit. For In-Vitro Diagnostic Use Catalog Number: NEA 103 | 3 | 08/20/2003 |
FEI # 1000513616 Perkinelmer Life Sciences, Inc. |
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