Last synced on 10 January 2025 at 11:05 pm

OptimMRI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230150
510(k) Type
Traditional
Applicant
RebrAIn, SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/21/2023
Days to Decision
183 days
Submission Type
Summary

OptimMRI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230150
510(k) Type
Traditional
Applicant
RebrAIn, SAS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/21/2023
Days to Decision
183 days
Submission Type
Summary