Medical Device Recalls
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1 result found
510(K) Number: K000238 |
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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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| HerpeSelect 1 and 2 Immunoblot IgG Kit, IB0900G Intended for qualitatively detecting the presence... | 2 | 08/17/2008 | Focus Diagnostics Inc |
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