Last synced on 14 November 2025 at 11:06 pm

3880 MRI Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K182900
510(k) Type
Traditional
Applicant
Iradimed Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
59 days
Submission Type
Summary

3880 MRI Patient Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K182900
510(k) Type
Traditional
Applicant
Iradimed Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
59 days
Submission Type
Summary