Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K063526 |
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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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ViroMax viral/bacterial filter. The filter reduces the risk of infection due to cross-contamination ... | 2 | 01/11/2012 | A M Systems Inc |
Xenon Diagnostic Circuit Kits labeled as "Xenon Diagnostic Circuit", "Xenon Circuit", and Needleless... | 2 | 06/03/2010 | Continental Medical Labs,Inc |
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