Medical Device Recalls
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1 result found
510(K) Number: K943705 |
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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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IMMULITE/IMMULITE 1000 Systems FOL Folic Acid, REF/Catalog Number LKFO1 (100 tests), Siemens Materia... | 2 | 12/24/2013 | Siemens Healthcare Diagnostics |
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