Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K090087 |
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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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MRidium 1145 Dose Reduction System (DERS) drug library kit. (This is an option for the MRidium 3860... | 1 | 08/02/2013 | Iradimed Corporation |
Iradimed Corporation MRidium MRI 1000 Series Infusion Sets, MRI Infusuui Set - Syringe Adapter Set, ... | 2 | 03/30/2023 | Iradimed Corporation |
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