Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K160006 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage... | 2 | 11/17/2021 |
FEI # 2022379 Fujifilm Irvine Scientific, Inc. |
| Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage... | 2 | 11/17/2021 |
FEI # 2022379 Fujifilm Irvine Scientific, Inc. |
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