Medical Device Recalls
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1 result found
510(K) Number: K862043 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DELFIA hFSH kit. In Vitro Diagnostic for the determination of hFSH in serum | 3 | 12/16/2016 | PerkinElmer Health Sciences, Inc. |
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