Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K133692 |
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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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IMRIS IMRI 1.5T AND 3T S System Product Usage: The IMRIS intraoperative MRI systems are traditio... | 2 | 05/04/2018 | Deerfield Imaging, Inc. |
Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated fo... | 2 | 03/11/2016 | Deerfield Imaging |
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