Medical Device Recalls
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1 result found
510(K) Number: K973742 |
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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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Package Insert which accompanies the Hematocrit and Metabolite QUALICHECK LEVEL 2 Quality Control of... | 3 | 08/02/2006 | Radiometer America Inc |
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