Last synced on 14 November 2025 at 11:06 pm

VisiRad XR

Page Type
Cleared 510(K)
510(k) Number
K223133
510(k) Type
Traditional
Applicant
Imidex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2023
Days to Decision
304 days
Submission Type
Summary

VisiRad XR

Page Type
Cleared 510(K)
510(k) Number
K223133
510(k) Type
Traditional
Applicant
Imidex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2023
Days to Decision
304 days
Submission Type
Summary