Medical Device Recalls
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1 result found
510(K) Number: K884544 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Factor VIII Chromogenic Assay, REF/Catalog No. B4238-40, Siemens Material Number (SMN) 10445729, IVD... | 2 | 12/22/2015 |
FEI # 2432235 Siemens Healthcare Diagnostics, Inc. |
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