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NeuroStar Advanced Therapy System (Version 3.7)

Page Type
Cleared 510(K)
510(k) Number
K230029
510(k) Type
Traditional
Applicant
Neuronetics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2023
Days to Decision
90 days
Submission Type
Summary

NeuroStar Advanced Therapy System (Version 3.7)

Page Type
Cleared 510(K)
510(k) Number
K230029
510(k) Type
Traditional
Applicant
Neuronetics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2023
Days to Decision
90 days
Submission Type
Summary