Medical Device Recalls
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1 result found
510(K) Number: K970220 |
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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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The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The Diamedix Is-anti-Sm Test Kit... | 2 | 06/26/2015 | Diamedix Corporation |
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