FDA 510(k) Applications Submitted by IRADIMED CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K172200 07/21/2017 3880 MRI Patient Monitoring System Iradimed Corporation
K090087 01/13/2009 MRIDIUM 3860 MRI INFUSION PUMP/MONITORING SYSTEM IRADIMED CORPORATION
K050301 02/08/2005 MRIDIUM 3850 MRI PUMP SYSTEM IRADIMED CORPORATION
K143369 11/25/2014 MRidium 3860+ MRI infusion Pump/ Monitoring System IRADIMED CORPORATION
K180903 04/06/2018 3880 MRI Patient Monitoring System Iradimed Corporation
K182900 10/16/2018 3880 MRI Patient Monitoring System Iradimed Corporation


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