Medical Device Recalls
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1 result found
510(K) Number: K133692 |
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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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| IMRIS IMRI 1.5T AND 3T S System Product Usage: The IMRIS intraoperative MRI systems are traditio... | 2 | 05/04/2018 |
FEI # 3010326005 Deerfield Imaging, Inc. |
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