Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061916 |
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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 ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both th... | 2 | 11/21/2012 | Innovative Magnetic Resonance Imaging Systems 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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