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MRidium 3860+ MRI infusion Pump/ Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K143369
510(k) Type
Traditional
Applicant
IRADIMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2016
Days to Decision
751 days
Submission Type
Summary

MRidium 3860+ MRI infusion Pump/ Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K143369
510(k) Type
Traditional
Applicant
IRADIMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2016
Days to Decision
751 days
Submission Type
Summary