Medical Device Recalls
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1 result found
510(K) Number: K051321 |
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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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A1CNOW+ with sampler 10-Test Kits (Product No: 3022), Metrika, Inc., Sunnyvale, CA 94085. (This tes... | 2 | 06/25/2015 | Metrika Inc |
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