Medical Device Recalls
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1 result found
510(K) Number: K931409 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| IMMULITE /IMMULITE 1000 Systems COR Cortisol, REF/Catalog Number LKC01, SMN 10381388, IVD. For in... | 2 | 10/23/2014 |
FEI # 2432235 Siemens Healthcare Diagnostics |
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