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Iradimed Corporation

7 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MRidium 3870 MRI Infusion Pump System (3870) (K242752)Iradimed Corporation2025-05-28
3880 MRI Patient Monitoring System (K180903)Iradimed Corporation2019-03-29
3880 MRI Patient Monitoring System (K182900)Iradimed Corporation2018-12-14
3880 MRI Patient Monitoring System (K172200)Iradimed Corporation2017-10-25
MRidium 3860+ MRI infusion Pump/ Monitoring System (K143369)Iradimed Corporation2016-12-15
MRIDIUM 3860 MRI INFUSION PUMP/MONITORING SYSTEM (K090087)Iradimed Corporation2009-04-07
MRIDIUM 3850 MRI PUMP SYSTEM (K050301)Iradimed Corporation2005-03-24

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Every clearance here is in the API, with alerts when new ones post.