Medical Device Recalls
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1 result found
510(K) Number: K983391 |
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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 2000/IMMULITE ® 2000 XPi OM-MA (CA125) | 2 | 05/04/2018 | Siemens Healthcare Diagnostics, Inc. |
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