Last synced on 12 October 2025 at 8:21 pm

iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221081
510(k) Type
Traditional
Applicant
First Source Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2022
Days to Decision
62 days
Submission Type
Summary

iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221081
510(k) Type
Traditional
Applicant
First Source Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2022
Days to Decision
62 days
Submission Type
Summary