Last synced on 20 December 2024 at 11:05 pm

XR90 (XR90-SYS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223125
510(k) Type
Traditional
Applicant
MediView XR, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2023
Days to Decision
283 days
Submission Type
Summary

XR90 (XR90-SYS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223125
510(k) Type
Traditional
Applicant
MediView XR, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2023
Days to Decision
283 days
Submission Type
Summary