Last synced on 25 January 2026 at 3:41 am

neuro42 MRI System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232644
510(k) Type
Traditional
Applicant
Neuro42, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2024
Days to Decision
162 days
Submission Type
Summary

neuro42 MRI System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232644
510(k) Type
Traditional
Applicant
Neuro42, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/2024
Days to Decision
162 days
Submission Type
Summary