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neuro42 MRI System

Page Type
Cleared 510(K)
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)
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