Medical Device Recalls
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1 result found
510(K) Number: K071388 |
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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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| GENTIAN Cystatin C Calibrator and Calibrator Kit, for the following models: 1. Gentian C E, Cysta... | 2 | 10/13/2020 | Gentian AS |
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