Medical Device Recalls
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1 result found
510(K) Number: K923212 |
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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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| SLIDEX Staph kit (250 Tests). The SLIDEX Staph-Kit is a rapid latex and red blood cell agglutinat... | 2 | 02/16/2012 | bioMerieux, Inc. |
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