Last synced on 14 November 2025 at 11:06 pm

3880 MRI Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K180903
510(k) Type
Traditional
Applicant
Iradimed Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2019
Days to Decision
357 days
Submission Type
Summary

3880 MRI Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K180903
510(k) Type
Traditional
Applicant
Iradimed Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2019
Days to Decision
357 days
Submission Type
Summary