Medical Device Recalls
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1 result found
510(K) Number: K991834 |
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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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Alere Cholestech LDX ALT AST Test Cassette, Model #12-788. For the in vitro quantitative determin... | 2 | 04/17/2013 | Alere San Diego, Inc. |
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