Last synced on 14 November 2025 at 11:06 pm

F3

Page Type
Cleared 510(K)
510(k) Number
K222998
510(k) Type
Traditional
Applicant
Acrew Imaging, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2023
Days to Decision
265 days
Submission Type
Summary

F3

Page Type
Cleared 510(K)
510(k) Number
K222998
510(k) Type
Traditional
Applicant
Acrew Imaging, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2023
Days to Decision
265 days
Submission Type
Summary